CA2272138C - Pyrazolopyrimidine and pyrazolopyridine compounds having crf antagonist activity - Google Patents

Abstract

Disclosed are compounds of the formula:

Description

PYRAZOLOPYRTMIDINE AND PYRAZOLOPYRIDINE COMPOUNDS
HAVING CRF ANTAGONIST ACTIVITY
This is a divisional application of Canadian Patent Application Serial No. 2,150,483 filed November 3, 1993.
The subject matter of this divisional application is restricted to pyrazolopyrimidine and pyrazolopyridine compounds of the formula I shown hereinunder in which A and R1 are taken together, and to pharmaceutical compositions containing them.
These compounds have corticotropin-releasing factor (CRF) antagonist activity.
It should be understood that the expression "this invention" or the like found in this specification encompasses the subject matter of both this divisional and parent applications.
CRF antagonists are mentioned in U. S. Patents Nos.
4,605,642 and 5,063,245 referring to peptides and pyrazolinones, respectively. The importance of CRF antagonists is set out in the literature, e. g. as discussed in U. S. Patent No.
5,063,245. A recent outline of the different activities possessed by CRF antagonists is found in M. J. Owens et al., Pharm. Rev., Vol. 43, pages 425 to 473 (1991). Based on the research described in these two and other references, CRF
antagonists are effective in the treatment of a wide range of diseases including stress-related illnesses, such as stress-induced depression, anxiety, and headache; abdominal bowel syndrome; inflammatory diseases; immune suppression, human immunodeficiency virus (HIV) infections; Alzheimer's disease;
gastrointestinal diseases; anorexia nervosa; hemorrhagic stress;
drug and alcohol withdrawal symptoms; drug addiction, and fertility problems.
The compound of formula I below wherein A is C=O, Rl is amino, R2 is methylthio, R3 is 2-chlorophenyl, and R4 is 2,4,6-trichlorophenyl is a commercial compound of no known utility.
The present invention relates to compounds of the formula:

-la-R., I
r,l and the acid addition salts thereof, wherein A is C=0 or S02, or A and Rl together with the carbons to which they are attached form pyrimidinyl or 5-pyridyl, each of which may be substituted by R5 which is hydrogen, C1-C6 alkyl, fluoro, chloro, bromo, hydroxy, amino, O(C1-C6 alkyl), NH(Cl-C6 alkyl), N(C1-C6 alkyl)(C1-C6 alkyl), 4-ethoxycarbonylpiperazinyl, SH or S(O)n(C1-C6 alkyl) wherein n=0, 1 or 2, wherein each C1-C6 alkyl may be substituted by from 1 to 3 substituents R6 which is hydroxyl, amino) C,-C3 alkoxy, dimethyfamino, diethylamino, methylamino, ethylamino, NH(C=O)CH3, fluoro, chloro, bromo or C,-C3 thioalkyl;
R, is hydrogen, C,-Ce alkyl, amino, O(C,-Ce alkyl), NH(C,-Ca alkyl), N(C,-Ce aikyl)(C,-Ce alkyl), wherein said C,-Ce alkyl may be substituted by from 1 to substituents Re as defined above;
RZ is hydrogen, C,-Ce alkyl, hydroxyl amino, O(C,-Ce alkyl), NH(C,-CQ alkyl), N(C,-Cs alkyl)(C,-Ca alkyl), SH, S(O)"(C,-Ce alkyl) wherein n = 0, 1, or 2, cyano, hydroxyl carboxyl or amido) wherein said alkyls may be substituted by one to three of hydroxyl amino, carboxyl amido, NH(C=O)(C,-Ce alkyl), N(C,-Cs alkyl)(C,-Ce alkyl}, (C=O)O(C,-Ca alkyl), C,-C, alkoxy, C,-C, thioalkyl, fluoro, bromo, chloro, iodo, cyano or vitro;
R, is phenyl, naphthyf, thienyl, benzothienyi, pyridyl) quinofyf, pyrazinoiyl) pyrimidyl, imidazolyl) furanyl, benzofuranyl, benzothiazolyl, isothiazolyi) benzoisothiazolyl) thiazolyl, isoxazolyi, benzisoxazolyi, benzimidazolyl, triazolyl) pyrazolyl, pyrrolyl) indolyi, azaindolyl, benzoxazolyi) oxazolyl) pyrrolidinyl) thiazolidinyl) morpholinyl, pyridinyl, tetrazolyl, or 9 to 12 membered bicycloalkyl, optionally containing one to three of O, S or N-Z wherein Z is hydrogen, C,-C4 alkyl, C,-C4 alkanoyl, phenyl or phenyfmethyi) wherein each one of the above groups may be substituted independently by from one to three of fluoro, chloro, bromo, C,-Ce alkyl, C,-Cs alkoxy, or tr'rfiuoromethyl, or one of cyano, vitro) amino, NH(C,-Ce alkyl), N(C,-C4 alkyl)(C,-C2 alkyl), COO(C,-C~ alkyl), CO(C,-C4 alkyl), SO=NH(C,-C, alkyl), SOzN(C,-C4 alkyl)(C,-Cz alkyl), SO=NHS, NHSOz(C,-C, alkyl)) S(C,-Ce alkyl}) SOz(C,-Ce alkyl)) wherein said C,-C~
alkyl and C,-Ce alkyl may be substituted by one or two of fluoro, chloro, hydroxy, amino, methylamino, dimethyiamino or acetyl; and R4 is phenyl, naphthyl, thienyl, benzothienyl, pyridyl) quinolyl, pyn3zinolyl, pyrimidyl, imidazoiyl, furanyl, benzofuranyl, benzothiazolyt, isothiazolyl, benzoisothiazolyl, thiazolyi) isoxazolyl, benzisoxazolyl, benzimidazolyl, triazolyf, pyrazolyi, pyrrolyl, indolyl, azaindoiyl, benzoxazolyl, oxazolyl, pyrrolidinyl, thiazolidinyl, morpholinyi, pyridinyl) tetrazolyl, or 3 to 8-membered cycloalkyi or 9 to 12-membered bicycloalkyl, optionally containing one to three of O, S or N-Z wherein Z is hydrogen) C,-C4 alkyl, C,-C,~ alkanoyl) phenyl or phenyimethyi, wherein each of the above groups may be substituted independently by from one to three of fluoro, chloro, bromo, trifluoromethyl, C,-Ce alkyl or C,-Ca alkoxy, or one of cyano) vitro, amino, NH(C,-C6 alkyl), N(C,-C4 alkyl)(C,-Cz alkyl), COO(C,-C4 alkyl), CO(C,-C~ alkyl), S02NH(C,-C4 alkyl), S02N(C,-C4 alkyf)(C,-C~ alkyl), SOZNHz, NH2SOs(C,-C,~ alkyl), S(C,-CQ
alkyl), S02(C,-Ce alkyl), wherein said C,-C, alkyl and C,-CQ alkyl may be su5stituted by one or two of fluoro, chloro, hydroxy, amino, methytamino, dimethytamino or acetyl;
provided that (1 ) R~ is not unsubstituted phenyl; (2) when R, is amino, R2 is methytthio, R4 is 2,4,6-trichiorophenyl, and A is C=O, then R, is not 2-chiorophenyf; and (3) R, and R~ are not both hydrogen.
More spedfic compounds of the formula I include those wherein R3 is phenyl substituted independently with one or two of fluoro, chloro, bromo, methyl, trifluoromethyl, vitro, C,-CQ alkyl, C,-Ce alkyioxy, S02NHz, SOZNH(C,-CQ
alkyl), SOZN(C, CQ alkyf)Z, or R3 is primary) secondary or tertiary alkyl of from 4-9 carbon atoms wherein said C4 Ce alkyl may contain from one to two double or triple bonds and may be substituted by from 1 to 3 substituents Ra which is hydroxy, amino, C,-C3 alkoxy) dimethytamino) diethylamino, methylamino, ethylamino, NH(C=O)CH3, fluoro, chloro, bromo, or C,-C, thioalkyl.
More specific compounds of the formula t are those wherein A is C=O, those wherein R, is amino) methytamino or dimethytaminQ; those wherein RZ is ethyl or methytthio and those wherein R4 is 2,4,6-trichlorophenyt, 2,4,&trimethylphenyl, 2,6-dichforo-4-trifluoromethyiphenyl or 4-bromo-2,6-dimethyiphenyl.
More specfic compounds of formula 1 further include those wherein R, is phenyl which may be substituted at positions 2 or 5 with one ar two of methyl, C2 Ce straight-chain or branched alkyl, trifluoromethyl, fluoro, chloro, bromo or vitro, those wherein A and R, together form a pyrimidine ring, such that the bicydic structure formed is pyrazolo[3,4-d]pyrimidine, and R5 is substituted at the 6 position; and those wherein R3 is phenyl substituted independently with one or two of fluoro) d~toro, bromo, methyl, trifluoromethyl, vitro, C,-Ce alkyl, C,-Ce alkyloxy) SOzNHZ, SOZNH(C,-Ce alkyl), or SOZN(C,-Caslkyl)Z, R, is 2,4,trtrichlorophenyl, 2,4,6-trtmethytptrenyl, 2.6-dichloro-4-trifluoromethyfphenyl or 4-bromo-2,6-dimethylphenyl, and RZ is methytthio, methyl or ethyl.
. More sped6c compounds of formula I also include those wherein R, is phenyl substituted independently with one or two of fluoro, chloro, bromo, methyl) trifluoromethyl, vitro, C,-Ca alkyl, C,-Ca alkyloxy, SOzNHZ, SOzNH(C,-CQ
alkyl), S02N(C,-CQ alkyl)Z, or R3 is primary, secondary or tertiary alkyl of firom 4-9 carbon atoms, wherein the C4-C9 alkyl may contain from one to two double or triple bonds and may be substituted by from 1 to 3 substituents R6 which is hydroxyl, amino C1-C3 alkoxy, dimethylamino, diethylamino, methylamino, ethylamino, NH(C=O)CH3, fluoro, chloro, bromo or C1-C3 thioalkyl; R4 is 2,4,6-trichlorophenyl, 2,4,6-trimethylphenyl, 2,6-dichloro-4-trifluoromethylphenyl or 4-bromo-2,6-dimethylphenyl; R1 is amino, methylamino or dimethylamino; and R2 is methylthio or ethyl.
Claimed in this divisional application are those compounds of the formula:

I

I-c \N/
Rl I

and pharmaceutically acceptable salts thereof, wherein A and Rl together with the carbons to which they are attached form pyrimidinyl or 5-pyridyl which may be substituted as defined above; and R2, R3 and R4 are as defined above.
The invention also relates to a composition for the treatment of illnesses induced or facilitated by corticotropin releasing factor which comprises a compound of the formula I
as defined above or the known compound of formula I wherein A
is C=O, R1 is amino, R2 is methylthio, R3 is 2-chlorophenyl, and R4 is 2,4,6-trichlorophenyl, in an amount effective in the treatment of said illnesses, and a pharmaceutically acceptable carrier, and to a composition for the treatment of inflammatory disorders, stress and anxiety related disorders including stress-induced depression and headache, abdominal bowel syndrome, immune suppression, HIV infections, Alzheimer's disease, gastrointestinal diseases, anorexia nervosa, hemorrhagic stress, drug and alochol withdrawal symptoms, drug -4a-addiction, and fertility problems, which comprises a compound of the formula I as well as the known compound, both as defined above in an amount effective in the treatment of said disorders, and a pharmaceutically acceptable carrier. More specific and most preferred compositions for the treatment of such illnesses and disorders comprise a more specific and most preferred compound of formula I as defined above.

The invention further includes a method for the treatment of illnesses induced or facilitated by corticotropin releasing factor by administering to a subject in need of such treatment a compound of formula I or the known compound, both as defined above, and a method for the treatment of stress and anxiety related disorders, including stress-induced depression and headache, abdominal bowel syndrome, inflammatory disorders, immune suppression, HIV infections) Alzheimer's disease, gastrointestinal diseases, anorexia nervosa) hemorrhagic stress, drug and alcohol withdrawal symptoms, drug addiction, and fertility problems) particularly depression, by administering to a subject in need of such treatment a compound of formula I
as well as the known compound, both as defined above. More spedfic and most preferred methods for the treatment of such illnesses and disorders comprise a more specfic and most preferred compound of formula I as described above.
Whenever reference is made herein to C,-Ce alkyl) a straight or branched chain alkyl of one to six carbon atoms is meant, such as methyl, ethyl) isopropyl or hexyl.
Whenever reference is made herein to C,-Ce alkyl, in the definition of R5 and R"
this indudes unsaturated Ci Ce alkyl, such as Ci Ce alkyl having one double or triple bond, C3 Ca alkyl having two double bonds, and C4 Ca alkyl having two triple bonds.
Whenever reference is made hereafter to a compound of formula I, this includes the known compound of formula I as described above.
Whenever R3 is a heterocyclic group, the attachment to A, defined above, is through one of the carbons in the heterocyciic group. Similarly, when R4 is a heterocydic group, the attachment to the nitrogen in the pyrazofe ring is through one of the carbons in the heterocyclic group.
Whenever reference is made herein to 3- to &membered cydoalkyl or 9- to 12 membered bicydoalkyl containing one to three of O, S or N-Z, It is understood that the oxygen and sulfur ring atoms are not adjacent to each other.
The compounds of the formula 1 wherein R, is amino or C,-Ce alkyl, and RZ is methytthio, having the formula II .(not shown), may be prepared from a compound of the formula R3- q -C -Rio II III
C
I
<SCH3)2 wherein R,o is cyano or C(O)(C,-CQ alkyl) and A and R3 are as defined above with reference to formula I, by reaction with a compound of the formula wherein R4 is as defined with reference to formula 1. This reaction is generally carried out in a polar solvent, such as a C,-Ca alcohol. The reaction temperature generally ranges from about 20 ° C to about 160 ° C, and is conveniently the refiux temperature of the reaction mixture.
The compounds of formula III may be prepared by treating a compound of the formula Ra_R-CH2Rio V
with a base such as sodium hydride, in the presence of carbon disulfide followed by reaction of the formed intermediate with methyl iodide in a reaction solvent such as dimethylsuffoxide.
The compounds of formula IV are readily available or may be obtained by methods known in the art.
The compounds of formula V may be prepared by known methods.
The compounds of the formula I wherein Rz is alkoxy) amino, or mono- or disubstituted amino may be prepared by using the above procedure with R4NHNH2 from the con-esponding compounds of the formula Ra-A-C-Rlo R3-p-C-Rio . (OR) . (NR~R~~)2 _7_ wherein A and R, are as defined with reference to formula I, R, o is as defined with reference to formula III, and R, R' and R" are each hydrogen or C,-CQ alkyl in accordance with the definition of Rz above.
The compounds of the formula I wherein R, is C,-Ce alkoxy or C,-CQ alkylthio and RZ is C,-Ce alkyl may be prepared from a compound of the formula z IX
R
i Ra wherein RX is chloro or bromo, RZ is C,-CQ alkyl, and R,, R4 and A are as defined above with reference to formula l) with a C,-Ce alcohol or C,-Cs mercaptan in the presence of a base. The reaction is generally carried out in a polar solvent such as ethanol or t-butanol at temperatures from about 20°C to about 160°C and conveniently room temperature.
The compounds of the formula IX may be prepared by treating a compound of the formula R
~3 ~N X
H 0 ~N~
Ra with a halogenating agent such as thiortyl chloride or bromide, or phosphorous oxychloride or pentachloride, or phosphorous oxybromide or pentabromide. The reaction may be carried out without a solvent or in an aprotic solvent such as methylene chloride, or dichloroethane at temperatures of about 0 ° C to about 100 ° C.
Compounds of formula X may be prepared by treating compounds of the formula II XI
/N
N

with an activated derivative of a carboxylic or sulfonic acid of the formula R,AOH, such as an acid chloride of the formula R3ACl wherein R, and A are as defined with reference to fom~uia i, in the presence of calcium hydroxide in an aprotic solvent such as dioxane as described in ,lensen, Acta Chem. Scand., 13, 1668-1670 (1959) at temperatures of from about 20°C to about 100°C. Compounds of the formula XI are known in the art.
The compounds of the formuta f wherein R, is C,-Ce alkoxy or C,-CQ alkyithio and R2 is C,-Ce alkylthio may be prepared from a compound of the formula XII
R Y \N/
Ra wherein R" is chloro or bromo and R3, R4 and A are as defined above with reference to formula I, with n C,-CQ alcohol or C,-Ce mercaptan in the presence of a base. The reaction is generally carried out in a polar organic solvent such as ethanol-or t-butanol at temperatures firom about 20 ° C to about 160 ° C, conveniently room temperature.
The compounds of the formula Xil may be prepared from a compound of the formula so XIII
H
i Ra -g-by reaction with a hafogenating agent such as thionyl chloride or bromide, or phosphorous oxychloride or pentachloride, or phosphorous oxybromide or pentabromide. The reaction may be carried out with a solvent or in ari aprotic solvent such as methylene chloride or dichloroethane at temperatures of about 0°C to about 100°C.
The compounds of the formula Xiil may be prepared by treating a compound of the formula ll xIV
/N
N

with activated benzoic or sutfonic acid derivatives) conveniently an acid chloride, in the presence of calcium hydroxide in an aprotic solvent such as dioxane as described in the above reference by Jensen.
The compounds of the formula XIV may be prepared by treating a compound of the formula R
z II XV
/N
N

wherein Rz is chloro, bromo with a C,-Ce mercaptan in the presence of a base.
The reaction is generally carried out in a potar organic solvent such as t-butanol at temperatures from about 20 ° C to about .160 ° C, convenierttiy the reflux temperatures of the reaction mixture.
The compounds of the formula XV may be prepared from compounds of the formula OH
II XV I
/N
N

with a halogenating agent such a thionyl chloride or bromide, or phosphorous oxychloride or pentachioride, or phosphorous oxybromide or pentabromide. The reaction may be carried out without a solvent or in an aprotic solvent such as methylene chloride or dichioroethane at temperatures of about 0 ° C to about 100 ° C.
The compounds of the formula I wherein R, is C,-Ca alkoxy or C,-Ca alkylthio and R2 is C,-CQ alkoxy may be prepared from a compound of the formula A Rz XVII
Rxx \N/
Ra wherein R,~,~ is chloro or bromo, R2 is C,-CQ alkoxy and R,, R4 and A are as defined above with reference to formula I, with a C,-Ca alcohol or C,-CQ mercaptan in the presence of a base. The reaction is generally carried out in a polar organic solvent such as ethanol or t-butanol at temperatures from about 20°C to about 160C) conveniently the refiux temperature of the reaction mixture.
The compounds of the formula XVII may be prepared from a compound of the formula ~ IN X V I I I
H 0 \N/
i Ra by reaction with a hslogenating agent such as thionyl chloride or bromide, or phosphorous oxychloride or pentachloride, or phosphorous oxybromide or pentabromide. The reaction may be carried out without a solvent or in an aprotic solvent such as methylene chloride, or dichloroethane at temperatures of about 0 ° C
to about 100°C.
The compounds of the formula XVIII may be prepared by treating a compound of the formula 1o II XIX
/N
N
Ra with an activated derivative of a carboxylic or sulfonic acid of the fomnula R3AOH, conveniently an acid chloride of the formula R3ACI wherein R, and A are as defined above with reference to formula I) in the presence of calcium hydroxide in an aprotic solvent such a dioxane as described by Jensen in the reference cited above.
The compounds of the formula XIX may be prepared by treating a compound of the above formula XV with an alcohol in the presence of a base. The reaction is generally carried out in a polar organic solvent such as ethanol at temperatures from about 20 ° C to about 160 ° C, conveniently the reflux temperatures of the reaction mixture.
The compounds of the formula I wherein R, is amino and R= is O(C,-Caalkyl) may be prepared by reacting a compound of the formula A 0(C1-C6 alkyl) 0 I I~ XX
/N
. / ~ R

wherein R,, R4 and A are as defined above with reference to formula i, with hydrazine in a solvent such as a C,-CQ alcohol, conveniently at the boiling point of the solvent.

The compounds of the formula XX may be prepared by treating a compound of the formula A OH

R

wherein R3, R4 and A are as defined above with reference to formula I, with an alkylating agent such as di(C,-Ce alkyl) sulfate, and a base such as sodium hydride, in a solvent such as dimethylsutfoxide.
The compounds of the formula XXI may be prepared by treating a compound of the formula OH

XXII
I
Ra '0 with an activated derivative of a carboxylic or sutfonic acid of the formula R,AOH such as an acid chloride of the formula R3ACI, wherein R3 and A are as defined with reference to formula I, in the presence of a lewis acid such as aluminum chloride in an aprotic solvent such as methylene chloride, dichloroethane, or tetrachloroethane, at temperatures of about 0°C to about 150°C.
The compounds of the formula XXII may be prepared by treatment of a compound of the formula OH
XXIII
H 2 N \N/

with phthalic anhydride in acetic acid at the boiling point of the solvent.
The compounds of the formula XXlll may be prepared by contacting cyanoacetyl chloride with R4NHNHZ in the presence of a base followed by heating the resulting hydrazide at refiux in alcoholic solution in the presence of a base.
The compounds of formula I wherein A and R, are taken together to form pyrimidinyl have the fomnula ,, r ,R2 iN XXIV
R 5 \N N~
Ra wherein Rz, R3, R4, and RS are as defined above with reference to formula I.
These compounds may be prepared by cyclization of a compound of the above formula I
wherein A is C=O and R, is amino with a compound of the formula I t wherein RS is as defined with reference to formula I. This reaction is generally carried out at 100 to 250°C, and conveniently at the reflux temperature of the compound XXV.
The compounds of formula I wherein A and R, are taken together to form 5-pyridyl have the formula I IN XXV I
\N/

Ra wherein R2, R3, R, and RS are as defined with reference to tonnula 1. These compounds may be prepared as shown in Reaction Scheme 1.
Reaction Scheme 1 R3-C-CH3 + CzH50C-CH2-CH-XXVII XXVIII
R3-C-CH2-C-CHz-CHRS-XXIX

13 ~ 15 _/G ~ ,CH
~~C~CH2 ~N --.
I I
,,,.~~ o' XxX
Ra R2 Ra ~C ~ Re H
0 R5'N'- CH2 N/ ~ R5 /N XXVI
0 R< II
Ra XXXI XXXII
The compounds of formula XXIX are prepared by reacting a ketone of the formula XXVII with a compound of the formula XXVIII in a suitable solvent such as tetrahydrofurane in the presence of a base such as sodium hydride. The reaction is conveniently carried out at the refiux temperature of the reaction mixture.
The compound XXIX is reacted with a compound of the formula RzC(OCH3), to form the compound XXX. The reaction is carried out in a suitable solvent such as ethyl acetate, conveniently at the reflex temperature of the reaction mixture. The wavy line --- in formula XXX indicates that either isomer of this compound is included, in accordance with accepted convention for indicating stereoisomers.
The compound XXXI is prepared by reacting compound XXX with a hydrazine of the formula H2NNHR~ wherein R, is as defined with reference to formula I.
The reaction is carried out in a suitable solvent such as ethanol, conveniently at the reflex temperature of the reaction mixture.
The compounds of formula XXVI wherein R5 is linked to position 6 is formed by first reacting compound XXXI with hydrazine hydrate in a suitable solvent such as ethanol, conveniently at the reflex temperature of the reaction mixture. The compound XXXII is separated from precipitated phthalhydrazide and taken up in an organic solvent such as toluene. The compound XXVI is formed by dehydrogenation of compound X)OCII with palladium over carbon.
Reaction Scheme 1 shows the preparation of compounds XXVl~wherein R5 is in the 6-position. A similar reaction sequence may be followed to prepare compounds XXVI wherein RS is in the 7-position by replacing compound XXVIII by a compound of the formula The compounds of formula I wherein A is C=O and R, and Rz are the same group R, may be prepared by reacting a B-ketone of the formula II II
R7 C~CH2~C~R7 with the hydrazine of the formula IV as defined above to form a pyrazole compound of the formula R 7 \N/
Ra The reaction proceeds at reflux in an appropriate solvent such as ethanol.
After bromination of the pyrazole compound, e.g. with bromine in acetic acid, to fom~ the corresponding 4-bromo derivative and conventional metallation, e.g, with t-butyl lithium, at -78°C in tetrahydrofuran, a suitably activated R3 carboxylic acid such as the acid chloride R,C(O)CI is added to give the desired compound I.

The compounds of formula 1 wherein A is C=O and R, and RZ are not the same) and wherein R, or Rs is attached through a CZH4 fragment) may be prepared from a pyranone of the fomnuia ii ,,/~,, xxxtv Rii ~z wherein R, is as defined above, and Rz is as defined above when R" is C; Ca alkyl which may be substituted by 1 to 3 of Re, or R2 is R, when R" is C; Ca alkyl which may be substituted by one to three of hydroxy, amino) carboxy) amido, NH(C=O)(C,-Ca alkyl), N(C,-Ce alkyl)(C,-Ca alkyl), (C=O)O(C,-Ca), C,-C3 alkoxy, C,-C3 thioslkyl) fluoro) bromo, chloro, iodo, cyano or vitro. The compound XXXIV is reacted with a hydrazine of the formula HZNNHR, wherein R4 is as defined above to form compounds of the formulae ~J~ ~ 3 ~ 3 ~C CH2CH(OH)R11 ~C Rz and ~ IN
R~ N/ R11-CH- N/

Ra OH Ra which on dehydration and hydrogenation result in compounds of the formulae 3 ~ 3 ~C C2H4R11 ~C Rz and N N

Ra R4 The compounds of the formula I wherein A is C=O and R2 is O(C,-CQ alkyl) may be prepared by reacting a hydrazine of the formula R4NHNHZ with a compound of the fomlula (A) in n suitable solvent OH
~0 C H 3 ~ IN
CH Ri N~

Ra (R) (B>
such as THF or methylene chloride and cyclization of the resulting hydrazide with heat to give the intermediate (B). This compound may be reacted with an activated carboxyclic acid derivative such as the acid chloride R3(C=O)CI in the presence of a Lewis acid such as aluminum trichloride in a solvent such as ethylene dichloride at temperatures of from about -10 ° C to about 80 ° C. The formed compound of formula I wherein RZ is hydroxy may be reacted with (C,-Ce alkyl)L wherein L is a leaving group such as chloro) bromo, or tosylate and C,-Ca alkyl may be substituted in accordance with the substituents in the definition of R2.
Those compounds of formula I wherein R, is C,-Ce alkylamino or di(C,-Ce alkyl)amino may be prepared from corresponding compounds of fomnula I wherein R, is amino. When R) is me~thylamino or dimethylamino, reaction is with a methyfating agent such as methyl iodide. When R, is Cz-Ce alkylamino or di(CZ Ce alkyl)amino, reaction is with an alkylating agent such as Cz-Ca alkyl-L wherein L is a leaving group such as chloro, bromo) tosyiate, or mesylate. Both the methyiation and the Ci Ce alkylation is in the presence of a base such as sodium hydride and a solvent such as tetrahydrofuran, dimethyl fonnamide or dimethyl suifoxide.
The acid addition salts are prepared in a conventional manner by treating a solution or suspension of the free base of formula I with one chemical equivalent of a pharmaceutically acceptable acid. Conventional concentration or crystallization techniques are employed in isolating the salts. Illustrative of suitable acids are acetic, lactic, succinic, malefic) tartaric, citric, giuconic, ascorbic, benzoic) cinnamic, fumaric, sulfuric, phosphoric, hydrochloric, hydrobromic, hydroiodic, sulfamic, sutfonic acids such as methanesutfonic, benzene suffonic, p-toluenesutfonic, and related acids.

The compound of the invention may be administered alone or in combination with pharmaceutically acceptable carriers, in either single or multiple doses.
Suitable pharmaceutical carriers include inert solid diluents or fillers, sterile aqueous solution and various organic solvents. The pharmaceutical compositions formed by combining the novel compounds of formula I and the pharmaceutically acceptable carriers are then readily administered in a variety of dosage forms such as tablets, powders, lozenges, syrups, injectable solutions and the like. These pharmaceutical compositions can, if desired, contain additional ingredients such as flavorings, binders, excipients and the like. Thus, for purposes of oral administration, tablets containing various excipients such as sodium citrate, calcium carbonate and calcium phosphate may be employed along with various disintegn~nts such as starch, alginic acid and certain complex silicates, together with binding agents such as poiyvinyipyrrolidone, sucrose, gelatin and acacia. Additionally, lubricating agents such as magnesium stesrate, sodium fauryi sulfate and talc are often useful for tabletting purposes. Solid compositions of a similar type may also be employed as fillers in soft and hard filled gelatin capsules.
Preferred materials for this include lactose or milk sugar and high molecular weight polyethylene glycols. When aqueous suspensions or elixirs are desired for oral administration, the essential active ingredient therein may be combined with various sweetening or flavoring agents, coloring matter or dyes and, if desired, emulsifying or suspending agents, together with diluents such as water, ethanol, propylene glycol, glycerin and combinations thereof.
For parenteral administration, solutions of the novel compound of formula ! in sesame or peanut oil, aqueous propylene glycol, or in sterile aqueous solution may be employed. Such aqueous solutions should be suitably buffered if necessary and the liquid diluent first rendered isotonic with sufficient saline or glucose.
These particular aqueous solutions are especially suitable for intravenous, intramuscular, subcutaneous and intraperitoneal administration. The sterile aqueous media employed are all readily available by standard techniques known to those skilled in the art.
Additionally, it is possible to administer the compounds of the present invention topically when treating inflammatory conditions of the skin $nd this may be done by way of creams, jellies, gels, pastes and ointments, in accordance with standard pharmaceutical practice.

The effective dosage for the compound of formula I
depends on the intended route of administration and other factors such as age and weight of the patient, as generally known to a physician. The dosage also depends on the illness to be treated, although in general the daily dosage will range from about 0.1 to 50 mg/kg of the body weight of the patient.
More specifically, the daily dosage for stress-induced illnesses will generally range from about 0.1 to 50 mg/kg of the body weight of the patient to be treated, for treatment of inflammatory diseases aboutØ1 to about 100 mg/kg will be needed, for Alzheimer's disease, about 0.1 to about 50 mg/kg, as well as for gastrointestinal diseases, anorexia nervosa, hemorrhagic stress, and drug and alcohol withdrawal symptoms.
The pharmaceutical composition may be put in a commercial package for practical use. Such commercial package normally comprises a container in which the composition is contained. The commercial package usually also comprises a written matter which says that the pharmaceutical composition can or should be used for the treatment described in this specification.
The methods far testing the compounds for formula I
for their CRF antagonist activity are according to the procedures of Endocrinology, 116, 1653-1659(1985) and Peptides, 10,179-188(1985) which determine the binding activity of a test compound to a CRF receptor. The binding activity for the compounds of formula I generally ranges from about 0.2 nanomolar to about 10 micromolar.

The following abbreviations are used in the Examples=
Ph=phenyl; iPr-isopropyl; HRMS=high resolution mass spectrum.
Example 1 A. 2-Bromo-2',5'-dimethylacetonhenone.
A mixture of 10.60 g (0.10 mol) of para-xylene and 16.53 g (0.105 mol) of a-bromoacetyl chloride 1n 300 mL of 1,2-dichloroethane was cooled in an ice bath under an atmosphere of dry N2 and treated portion wise with 14.15 g (0.106 mol) of aluminum chloride. The reaction mixture was stirred for 30 minutes at 0-5°C and then for 2.5 hours at room temperature. The mixture was then poured onto ice and the aqueous layer was acidified with concentrated HC1. The organic layer was separated and the aqueous layer was extracted twice with methylene dichloride. The combined organic extracts were dried with brine solution and With magnesium sulfate. The solvent was evaporated to give 23.87 g of an amber oil which was for use in the next reaction without further purification.
B. 2-Cvano-2',5'-dimethy_lacetophenone.
The product of the above reaction (approximately 0.10 mol) was dissolved in 300 mL of ethanol and was treated with a solution of 16.25 g (0.25 mol) of potassium cyanide in 30 mL
of water and the resulting mixture was refluxed for 90 minutes. After -20a-cooling) the ethanol was stripped from the mixture on the rotary evaporator and the residues were made slightly acidic with concentrated hydrogen chloride. The product was extracted into ethyl acetate using precautions to avoid escape of hydrogen cyanide. The organic extracts were dried with brine and with magnesium sulfate and evaporated to a gummy semi-solid. This was triturated repeatedly with hot hexane which, on cooling, deposited needles to give the desired product, 8.50 g (4996 for the two reactions), m.p. 75 - 76°C.
C. 3,3-Bis-methytthio-2-(2.5-dimethylbenzoyll-acrylonitrile.
A solution of 4.96 g (28.6 mmol) of 2-cyano-2',5'-dimethylacetophenone in 120 mL of dry dimethyl sulfoxide and 3.43 mL (57.3 mmol) of carbon disulfide in a flame-dried 3-neck round bottom flask under dry nitrogen was stirred at 15 -18 ° C while 1.41 g (58.7 mmoi) of oil free sodium hydride was added in 5 portions. The resulting deep red solution was stirred for 1 hour at 18 ° C and then cooled to 15 ° C whereupon 3.92 mL (8.95 g, 63.0 mmol) of methyl iodide was added dropwise. The temperature rose to about 22 ° C during the addition. After stirring for 2 hours at room temperature, the reaction mixture was poured into cold water and the aqueous layer was extracted three times with ethyl acetate. The combined extracts were washed three times with water and then dried with brine and magnesium sulfate) Evaporation gave 8.96 g of the title compound as a heavy on3nge oil which crystallized in the refrigerator. The analytical sample crystallized from ethanol, m.p. 74.5 - 75.5°C.
D. 5-Amino-1-(2.6~iichloro-4-trilluoromethylahenH)-4-12.5~iimethyfbenzoyil~-methvithioavrazole.
A suspension of 7.94 g (28.6 mmol) of the product of step C and 7.01 g (28.6 mmol) of 2,6-dichioro-4-trifluoromethylphenylhydn3zine in 100 mL of ethanol was heated at reflux for 2 hours, solution occurring as the reactjon mixture was warmed:
Then the ethanol was mostly removed on the rotary evaporator and the residues were partitioned between dilute aqueous hydrogen chloride solution and ethyl acetate. The organic phase was washed once with water and with brine, then dried with magnesium sulfate and treated with decoforizing carbon. The flftered solution was evaporated and the residues crystallized from 10:1 hexane/ethyl acetate to give 12.00 g (8896) of the title product in two crops, m.p. 130 - 132°C.

' -22-Example 2 5-Methyiamino-4.-t2-chlorobenzoyl)-3-methylthio-l-(2.4.6-trichlorophenyl)pYrazole and 5-dime~thytamino-4-(2-chtorobenzoyll-3-methvtthio-1-(2.4.6-trichlor~phenyf)-pyrazole.
A mixture of 0.50 g (1.16 mmol) of 5-amino-4-(2-chlorobenzoyl}-3-methytthio-1-(2,4,6-trichlorophenyi)pyrazole in 5 mL of tetrahydrofuran was treated with 50 mg (1.16 mmol} of sodium hydride and stirred at room temperature for 30 minutes. Then 0.75 ml (1.71 g, 12.0 mmol) of methyl iodide was added dropwise and the reaction mixture was stirred for 60 minutes at room temperature. The reaction mixture was then quenched with water and the products were extracted into ethyl acetate.
Concentration of the dried solution and chromatography on silica gel with mixture of hexane and ethyl acetate gave the less polar dimethylamino title compound (300 mg, 5496) as a white foam. Anal. Calcd. for C,eH~50N3SCl,: C, 48.02; H, 3.18; N, 8.88. Found: C, 47.84;
H, 3.09; N, 9.01.
The more polar monomethyl title compound was isolated from the column in like manner as a white foam (34 mg, 696). Anal. Calcd. for C,BH"ON3SCI4: C, 46.88;
H, 2.84; N, 9.11. Found: C, 46.54; H, 2.89; N, 9.07.
Example 3 5-Amino-4-(2-methoxybenzoyl)-3-methytthio-1-(2.4.6-trichloroahenyi pyrazole.
To a solution of 2-methoxyphenylmagnesium bromide prepared from 18.7 g (0.10 mol) of 2-bromoanisole and 2.43 g (0.10 mol) of magnesium turnings in ether under dry nitrogen was added 1.6 g (5.0 mmol) of 5-amino-4-cyano-3-methytthio-(2,4,6-trichlorophenyl)pyrazoie and the resulting mixture was stirred and refluxed for 16 hours. Upon cooling, the reaction was decomposed with 50 mL of saturated ammonium chloride solution. The organic phase was extracted with aqueous hydrogen chloride and the acidic extract was treated with 10 mL of concentrated hydrogen chloride and heated at 80 - 90 ° C for 10 minutes after which the mixture was cooled and made alkaline. Extraction with methylene dichloride and chromatography of the extracts with mixtures of hexane and ethyl acetate gave 313 mg (1496) of the title compound, m.p. 200-202 ° C. Anal. Calcd, for C, ~H,4OzN,SCI,: C) 48.82;
H, 3.18; N, 9.49. Found: C, 48.54; H, 3.32; N, 9.09.

Example 4 A. 5-Amino-3-methyl-1-(2.4,6-trichloroohenvi)p~razole.
To a solution of 0.51 g (22.0 mmol) of sodium in methanol was added 1.66 g (20.0 mmol) of 5-methylisoxazofe. The reaction mixture as refiuxed for 8 hours and then stirred overnight at room temperature. Then 4.23 g (20.0 mmol) of 2,4,6 trichlorophenylhydrazine was added and the reaction mixture was again refluxed for 4 hours. A second portion of sodium in methanol was added and reflux was continued for 24 hours. The reaction mixture was taken up with ether and dilute hydrogen chloride. The organic extracts were washed with dilute hydrogen chloride and brine, and then dried with magnesium sulfate and evaporated to give crystals, m.p.

134 ° C. Analysis of this material, particularly two CN bands in the IR
spectrum at 2190 cm-' and 2250 cm'' , revealed it to be a mixture of the cis- and tn3ns-isomers of 1-cyanoacetone-2,4,6-trichiorophenyfhydrazone. This material was suspended in methanol and treated with 10.0 mmol of sodium methoxide in 5 mL of methanol.
After 5 minutes at room temperature, water was added to crystallize the product which was filtered off and washed well with water. After sir drying, the product weighed 2.21 g (4096) and melted at 134.0-135.5 ° C. Despite the similarity in melting points, the latter material was distinctly different from the former, having an R, of 0.67 vs.
0.78 for the intermediate on silica get TLC plates developed with 1:1 hexane ethyl acetate and a distinctly different 300 MHz proton NMR spectrum.
B. 5-(2-Chlorobenzamido)-4-(2-chlorobenzoyl~-3-methyl-1-(2.4.6-trichlorophenyl)pyrazofe.
A suspension of 2.34 g (17.50 mmol) of aluminum trichloride in 20 mL of 1,1,2,2-tetrachloroethane was treated with 2.02 mL (2.78 g, 15.9 mmol) of 2-chlorobenzoyl chloride and the resulting solution was stirred for 20 minutes at room temperature.
Then 2.00 g (7.23 mmol) of the product of Step A was added and the reaction mixture was reiiuxed for 16 hours. The cooled reaction mixture was poured over ice and the insolubles were littered off and washed with ethyl acetate. The organic layer was separated and the aqueous was washed twice with ethyl acetate. The combined organic layers were dried over magnesium sulfate and evaporated. The residues were chromatographed on silica gel, eluting with 4:1 hexane ethyl acetate to give 2.05 g (5196) of the title product, an amorphous foam. Anal. Calcd. for C~'H,,~O~N3Cl5: C, 52.06; H, 2.55; N, 7.59. Found: C, 52.11; H, 2.57; N, 7.27.

C. 5-Amino-4-(2-chforobenzoyll~-methyl-1-(2.4.6-trichlorophenyilpyrazole.
A solution of 1.94 g (3.50 mmol of the product of Step B in 20 mL of glacial acetic acid was treated with 20 mL of 4896 hydrogen bromide and stirred at reflux for 8 hours. The cooled reaction mixture was treated with water to crystallize the product which was separated by flttration, washed with water and air dried to give the title product, 1.45 g (10096)) m.p. softens about 210°C and melts at 222°C. Anal. Calcd.
for C"H" ONsCl4: 412.9656. Found: 412.9722.
F~cample 5 5-Methylamino~-(2-chlorobenzoyll~-methyl-1-(2.4.6-trichtorophenyl)pyrazafe and 5-dimethyiamino-4.-!2-chlorobenzo~rl)-3-methyl-1-l2.4,6-trichlorophe~l)pyrazole.
A solution of 0.208 g (0.5 mmol) of the compound of Example 4C in 20 mL of tetrahydrofuran (THF) was stirred in an ice/water bath while 5.0 mL of 1.0 M
sodium hexamethyfdisilazide in THF was added followed by 0.5 mL (1.14 g, 8 mmol) of methyl iodide. The reaction mixture was then stirred overnight at room temperature.
The reaction mixture was poured into water and the products were extracted into ethyl acetate, dried and concentrated. The residues were chromatographed on silica gel using 5:1 hexan%thyl acetate as eluent to give the less polar dimethyfamino title compound, 52 mg (2396)) m.p. 10&109°C (ether/pentane).
The more polar product likewise crystallized from etheNpentane to give 39 mg (1896) of the monomethylamino title compound, m.p. 174-175°C.
Example 6 5-amino-1-12.6-dichloro-4-trifluoromethylohenvll-4-(2.5-dimethylbenzoyll-3-(n-propyl~pYrBZOIe.
A solution of 0.52 g (3.0 mmol) of 2,5-dimethylbenzoylacetonitrile, 0.45 g (3.0 mmol) of trimethylorthobutyrate and 0.632 g (0.58 mh 6.2 mmol) of acetic anhydride in 5.0 mL of ethyl acetate was refluxed overnight and then cooled. The solvents were removed in vacuo and the residues were dissolved in 10 mL of ethanol. One-half of this solution, containing 1.5 mmol of 1-cyano-1-(2,5-dimethylbenxoyl)-3-methoxy-1-pentane was mixed with 0.7 mL (0.51 g, 5.0 mmol) of triethylamine and 0.37 g (1.50 mmol) of 2,6-dichioro-4.-triftuoromethyiphenylhydrazine and refluxed for 2.5 hours. The reaction mixture was cooled and partitioned between dilute hydrogen chloride and efhyl acetate.
The organic phase was washed with water and then dried with brine and with magnesium sulfate. The solvent was evaporated to give an oil which was chromatographed on silica gel by the flash method eluting with 4:1 hexane/ethyl acetate to give the title compound as an amorphous foam. Anal. Calcd. for Cz2H2oON3CIzFj, 469.0935. Found: 469.0889.
Example 7 A. 5-Amino-3-hvdroxy-1-12.4.6-trichloroahenvl)-cvrazole.
Cyanoacetic acid (8.5 g, 0.10 mol) in 200 mL of dry ether was treated with 20.8 g (0.10 mol) of phosphorous pentachloride, warmed briefly to reflux and let cool to room tempen3ture at which time all of the phosphorous pentnchloride, had dissolved.
After a small amount of insoluble material was removed by filtration, the ether was removed on the rotary evaporator. Then 100 mL of toluene was added and stripped to remove phosphorous oxytrichloride. The residual pale yellow oil was immediately dissolved in 50 mL of cold methylene dichloride and added to a cold suspension of 21.15 g (0.10 mol) of 2,4,6-trichlorophenylhydrazine in 14.0 mL of triethylamine and 100 mL of methyiene dichloride, keeping the temperature below 20 ° C by use of an ice bath.
The reaction mixture was allowed to warm to room temperature and stirred for one hour. Then 500 mL of cold water was added. The precipitated solid was filtered and washed with water and with a little methylene dichloride to give the intermediate 2-cyano-N-(2,4,6-trichlorophenyl)acethydn3zide, 14.92 g (5496)) m.p. 166-168°C. Anal.
Calcd. for CeHaON3: C, 38.81; H, 2.17; N, 15.09. Found: C, 38.83; H, 2.06; N, 14.81.
This material (14.92 g, 53 mmol) was dissolved in a solution of 2.80 g (0.12 mol) of sodium in 200 mL of methanol and refluxed for 4 hours. After stirring overnight at room temperature, the methanol was mostly evaporated and the residues were poured into water. The aqueous layer was extracted with ether and was then acidfied with concentrated hydrogen chloride. The product was extracted into ethyl acetate.
The extracts were dried with brine and magnesium sulfate and evaporated to give a foam which crystallized from ether to give 12.28 g (9396) of the title product, m.p. 221 -223 ° C. Anal. Calcd. for CeHeON,: C, 38.81; H, 2.17; N, 15.09. .Found:
C, 38.81; H, 2.16; N, 14.84.
B. 3-Hydroxy-5-ahthalimido-1-12,4.6-trichlorophenyl)pvn~zole.
A mixture of 4.50 g (18.0 mmol) of the compound of Step A and 2.81 g (19.0 mmol) of phthalic anhydride in 40 mL of glacial acetic acid was refluxed for 4 hours and stirred overnight at room temperature. About two volumes of water were added dropwise and the resulting solid was filtered and washed with water. The damp solid was taken up in a little ethanol) filtered and washed with a little ethanol and ether) and air dried to give the title compound, 5.11 g (6996), m.p. 295 - 298 °
C(dec). Anal. Calcd.
for C"H803N,C1,: C, 49.97; H, 1.97; N, 10.28. Found: C) 49.28; H,=1.95; N, 10.06.
C. 4-(2-Chlorobenzoyll-3-hydroxy-5-phthalimido-1-(2.4.6-trichlorophenYl, pyrazole.
Aluminum trichloride (2.34 g) 17.6 mmol) was added to a solution of 2-chlorobenzoy) chloride in 60 mL of 1 ( 1,2,2-tetrachloroethane and the resulting mixture was stir-ed for 30 minutes at room temperature. Then 2.87 g of the compound of Step B was added all at once and the reaction mixture was refluxed overnight. The cooled mixture was poured into water and the aqueous phase was extracted three times with ethyl acetate. The organic extracts were dried with brine and magnesium sulfate and evaporated to give a red oil which was taken up in methanol and crystallized to give the title compound, 2.97 g (7796), m.p. 245 - 246°C.
D. 4-(2-Chlorobenzoyl)-3-ethoxy-5-phthalimido-1-(2.4.6-trichloroahenyl)pyrazole.
A solution of 0.55 g (1.0 mmol) of the compound of Step C in 10 mL of dry dimethyl sutfoxide was treated portionwise with 36 mg (1.5 mmol) of sodium hydride and the resulting mixture was stirred for 30 minutes at room temperature. Then 0.21 mL (0.25 g, 1.61 mmol) of diethyl sulfate was added and the reaction mixture was stirred for one hour at room temperature. The reaction mixture was poured into water and the product was extracted into ethyl acetate. The extracts were washed with water and dried with brine and magnesium sulfate, and evaporated to a gum. The product was crystallized from boiling ethanol to give the product (230 mg, 4096) as fine crystals, m.p. 215 - 216°C.
E. 5-Amino-4-~2-chlorobenzoyl)-3-ethoxy-1-(2.4.&trichlorophenyl)pvrazole.
A suspension of 184 mg of the compound of Step D in 10 mL of ethanol was treated with 0.5 mL of 5596 hydrazine hydrate and refiuxed for 1 hour. Solids in the cooled reaction mixture were filtered off and discarded and the filtrate was evaporated to a gum which was triturated with ether and filtered. The filtrate was again evaporated to a foam which was shown to be 104 mg of the analytically pure title compound. Anal.
Calcd. for C,sH,3O2N,Cl4: C) 48.57; H, 2.94; N, 9.44. Found, C) 48.41; H, 2.52; N, 9.43.

Example 8 5-Dimethrfamino-4-l2~hlorobenzovi)~-methoxy-1-(2.4,6~richlorophenyi)pyrazole.
A solution of 60 mg (0.14 mmol) of 5-amino-4-(2-chlorobenzoyl)~-methoxy-1-(2,4,6-trichlorophenyl) pyrazole prepared according to Example 7 in 5 mL of dry dimethyt sutfoxide was treated with 22 mg (0.88 mmol) of oil-free sodium hydride to give 8 yellow solution. After i hour at room temperature, 0.2 mL (0.46 g) 3.21 mmot) of methyl iodide was added. After stirring for 5 hours, the reaction mixture was poured into water and the product was extracted into ethyl acetate. After drying with brine and magnesium sulfate, the solvent was removed to give the title product as a one-spot foam. ' H-NMR (COCt,): 2.77 (6H, s), 3.63 (3H, s)) 7.24 - 7.42 (4H, m), 7.48 (2H) s).
Example 9 A. 3.3-Bis-ethoxy-2-j3-trifluoromethylbenzoyl)-acrylonitrile.
Sodium (0.126 g, 5.5 mmol) was dissolved in 15 mL of ethanol and 20 mL of dioxane was added followed by 1.59 g (5.0 mmol) of 3,3-bis-methytthio-2-(3-trifluoromethylbenzoyl)-acryfonitrile and the reaction mixture was refluxed for 4 hours and let stir overnight at room temperature. This compound was relatively unstable to aqueous conditions and was not isolated as such. Instead, an aliquot of the mixture was stripped and the product was identified by 300 MHz proton NMR: NMR (DMSO-dQ): 1.14 (6H, tJ = 7), 3.45 (4H, q, J = 7)) 7.44 - 8.16 (4H) m).
8. 5-Amino-1-12.6-dichloro-4-trifluoromethylphenyl)-3-ethoxy-4-(3-trifiuoromethylbenzoy~l pyrazole.
An aliquot of the above solution of step A containing approximately two mifiimofes of 3,3-bis-ethoxy-2-(3-trifluoromethyfbenzoyf)acrylorirtrile was reacted with 0.49 g (2.0 mmol) of 2,6-dichforo-4.-trifluoromethylphenylhydrazine in 10 mL
of ethanol under reflux overnight. The cooled mixture was poured into dilute hydrogen chloride (HCI) and the product was extracted into ethyl acetate (EtOAc), washed with water and brine, and dried over magnesium sulfate (MgS04). Chromatography on silica gel with 4:1 hexane/EtOAc gave the title product, 320 mg (3196), m.p. 77 - 78 °
C from pentane.
Example 10 _ 5-Amino-1-(2.6-dichloro-4-trifluoromethyfphenyl)-4-(2,5-dimethylbenzoyl)-3-ethoxypyrazole.
A solution of 0.26 g (1.5 mmol) of 2,5-dimethylbenzoyiacetonitrile, 0.34 mL
(0.31 g, 1.60 mmol) of tetraethylorthocarbonate and 0.30 mL (0.33 g, 3.20 mmol) of acetic anhydride in 10 mL of EtOAc was refluxed overnight. The solvent was evaporated and mL of absolute ethanol was added and then stripped. The residues were dissolved in 10 mL of ethanol, 368 mg (1.5 mmol) of 2,6-dichloro-4-trifluofomethyiphenyl-hydrazine and 0.7 mL (0.51 g, 5.0 mmol) of triethylamine were added, and the mixture 5 was refluxed for 90 minutes. The mixture was poured into water, extracted with EtOAc and the organic extracts were washed with dilute HCI and brine, and dried over MgS04.
Evaporation gave a gum which was chromatographed on silica gel with 4:1 hexane/EtOAc to give the title product which crystallized from pentane, 15 mg (296), m.p. 99 - 101 °C.
10 Example 11 1-(2.6-Dichloro-4-trifluoromethylphen~)-5-methyl-4-(3-methylbenzoyl)-3-methylthiopvrazole.
A solution of 2.97 g (16.9 mmol) of 4-(3-methylphenyi)butane-2,4-dione and 4.04 mL (5.14 g, 67.6 mmol) of carbon disulfide in 60 mL of dry dimethy) sutfoxide was treated portionwise with 0.89 g (37.1 mmol) of oil free sodium hydride at 15 -18 ° C.
After stirring 30 minutes, 2.31 mL (5.27 g) 37.1 mmol) of methyl iodide was added dropwise and the reaction mixture was allowed to stir at room temperature for 1 hour.
It was then poured into water and the product was extracted into ether, backwashed with water and dried over MgS04 to give 4.30 g (9196) of an oil which crystallized in the refrigerator overnight, m.p. 44 - 46 ° C. ' H-NMR (CDCl3): 2.16 (3H, s), 2.38 (6H, s), 2.72 (3H, s), 7.26 - 7.38 (2H, m), T.58 - 7.T4 (2H, m). A mixture of 1.95 g (6.96 mmol) of 3,3-bismethytthio-2-(3-methylbenzoyl)-2-acetyiethene and 1.71 g of 2,6-dichloro-4-trifluoromethylphenylhydn3zine in 20 mL of ethanol was refluxed for 6 hours and then stirred at room temperature for 48 hours. The reaction mixture was poured into dilute HCI solution and the product was extracted into EtOAc. The solution was dried and concentrated and the residues were chromatographed on silica gel with 10:1 hexane/EtOAc to give the title product which crystallized from pentane, 1.67 g (5296), m.p. 103 - 104°C.
Example 12 . 5-Amino-1-(2.6-dichloro-4-trifluorometylphenyll-4-(5-f3-h~droxyaropyll-2-methylbenzoyl)-3-methyfthiopyn3zole.
A solution of 0.530 g (1.0 mmol) of 5-amino-1-(2,6-dichloro~-trifluoromethylphenyl)-4-(5-[t3-methoxycarbonylethylJ-2-methylbenzoyl)-3-methytthiopyrazole in 10 mL of THF was cooled in an ice bath while 1.33 mL of a 1.5 M solution of DIBAL in THF was added. The reaction mixture was warmed to room temperature and then quenched with water. The product was extracted into EtOAc, dried and concentrated. The residues were chromatognsphed on silica gel using mixtures of hexane/EtOAc to elute the title product which was isolated as an amorphous foam) 174 mg (3496). Anal. Calcd. for CZ2HZ°O=N3SCI2F3: C, 50.97; H, 3.88; N, 8.10. Found, C, 51.10; H, 3.96; N, 7.60.
Example 13 f5-Amino-l-(2.6-dichloro-4-trifluoromethylphenyil-3-methyisulfonyl-1 H~yrazol-yl]-(2,5-dimethylphenvl)methanone.
To a solution of 200 mg (0.42 mmol) of [5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl~3-methylsulfanyl-1 H-pyrazol-4-yl]-(2,5-dimethylphenyl)methanone in 10 mL of THF was added 0.176 g (2.10 mmol) of anhydrous sodium bicarbonate followed by a solution of 145 mg (0.42 mmol) of 3-chloroperoxybenzoic acid in 8 mL
of THF. After two hours at room temperature, 0.5 g of sodium bicarbonate and an additional 290 mg (0.84 mmol) of 3-chioroperoxybenzoic acid was added. The reaction mixture was heated briefly to 50 ° C, let cool and stirred overnight at room temperature.
The reaction mixture was added to water and the product was extracted into ethyl acetate. The organic extracts were washed with dilute sodium bicarbonate solution and then dried and evaporated. The title compound was crystallized from ether to give 150 mg (7096 yield) of colorless crystals, m.p. 193.5 - 194.5°C
Example 14 The following compounds in Tables 1 and 2 were prepared according to the indicated Example.

Ri2 Rli 0=C
1o R1 N/N
Ris Ri3 Process R, RZ R, 3 R, 4 R, 6 R" R, ~ Physical Data of (m.p. in C) Example amino SCH3 2-CI 4-CI 6-CI 2-CI H m.p.178-180 1 , amino SCH3 2-CI 4-CI 6-CI H H m.p.178-180 amino SCH, 4-CF3 H H 2-CI H m.p.150-153 n amino SCH, 2-CI 4-CI 6-CI 2-F H m.p.204-206 NHCH3 SCH, 2-CI 4-CI 6-CI 2-CI H m.p.135-137 N
N(CH3)z SCH3 2-CI 4-CI 6-CI 2-CI H m .p.

N(CH3)Z CH3 2-CI 4-CI 6-CI 2-CI H m.p.220-222 i ' amino SCH3 2-CF, H H 2-CI H m.p.186-188 amino SCH3 2-CI 4-CI 6-CI 2-cyclopropylH m.p.165-amino SCH3 2-CI 4-CI 6-CI 4-CH, H m.p.230-232 amino SCH3 2-CI 4-CI 6-CI 2-CI 4-CI m.p.
Amorphous. 1 Anal. Calc'd for C17H10N30SCI5:

C, 42.39; H, 2.09; N, 8.72. Found:

C,41.94; H, 2.06;
N, 8.07.

N(CH3)Z CH3 2-CI 4-CI 6-CI 2-CI H m.p.108-109 NHZ SCH3 2-F 4-F 6-F 2-CI H m.p.156-158 I

Process R, Rz R,3 R,4 R,s R" R,z , Physical Data of (m.p. in C) Example N(CH3)z SCH, 2-CI 4-CI 6-CI 2-F H m.p.
Amorphous. 2 HRMS for .

Caic'd: 466.9984 Found: 456.9990 n NH2 SCH, 2-CI 6-CI H 2-F H m.p .

NHZ SCH, 2-F 4-F H 2-CI H m.p.147-150 N(CH3)z SCH, 2-CI 4-CI 6-CI 3-CI H m.p.121-125 2 ( w NHZ NHCH, 2-CI 4-CI 6-CI 2-CI H m p .
.

NHz SCH, 2-CI 4-CI 6-CI 2-OCH, H m.p.200-202 NH2 SCH, 2-CI 6-CI 4-CF3 2-CI H m.p.207-210 NH(CH2)30CeH5SCH3 2-CI 6-CI 4-CI 2-CI H m.p.
Ambrphous. 5 Anal. Calcd.
for C26H21 N3O2SCI4:

C, 53.71; H, 3.64; N, 7.22. Found:
C, 53.57; H, 3.41;
N, 7.46.

NHZ SCH, 2-CI 6-CI 4-CI 3-CH3 H m.p.178-180 ~ i NHZ SCH3 2-CI 6-CI 4-CF3 3-CI H m.p.149-151 NHz SCH, 2-CI 6-CI 4-CF3 3-CH3 H m.p.150-153 i Process .R, Rz R,3 R)4 R,s R" R,2 Physical Data of (m.p. In C) Example I N(CH3)z SCH3 2-CI 6-CI 4-CF3 3-CI H m.p. 120-122 2 , NHS SCH3 2-Cl 6-CI 4-CI 3-CF, H m.p.158-160 NHCHZCOOH SCH, 2-CI 6-CI 4-CI 2-CI H m.p. > 250 n HRMS for C19H13N3O3SC14:

Calcd: 525.9930 Found: 525.9348 NHZ SCH3 2-CI 6-CF3 4-CI 3-CF3 H m.p.
Amorphous. 1 , Anal. Calcd.
for C19H11 N30SCI2F6: ~ o C, 44.30; H, o 2.15; N) 8.15. Found:
C, 44.51; H, 2.29;
N, , 7.98 NHz SCH3 2-CH3 4-CI H 2-CI H m.p.125-129 NHZ SCH3 2-CH3 4-CI H 3-CI H m.p.112-115 NHS SCH3 2-CI 4-CF3 6-CI 2-CH3 5-CH3 m.p.130-132 NHZ SCH3 2-CH3 6-CH3 H 3-C! H m.p.148-151 i Process R, Rz R" R,4 R,5 R" R,z Physical Data of (m.p. In C) Example N(CH3)~ SCH3 2-CI 4-CF3 6-CI 3-CF3 H m.p.
Amorphous. 2 Anal. Calcd. for C21 H15N30SCI2F6:

C) 46.50; H, 2.78;
N, 7.74. Found: C, 46.75; H, 2.93;
N, o 7.58 N
N

J
NH2 SCH3 2-CI 4-CF3 H 3-CI H m.p. t24-__ NHZ SCH3 2-CH3 6-CH3 H 3-CI H m.p.139-142 w ~o NHZ SCH3 2-CI 4-CI 6-CI 2-CH 5-CH m.p.182-184 1 ~

CH3 SCH3 2-CI 4-CI 6-CI 3-CH3 H m.p.116-117 NHZ SCH3 2-CH3 4-CI 6-CH3 3-CF, H m.p.
Amorphous. 1 Anal. Calcd. for C20H17N30SCIF3:

C, 54.48; H) 3.88;
N, 9.53. Found: C) 54.60; H) 3.91;
N) 9.08 Process R, Rz R,3 R,4 R,6 R" R,z Physical Data of (m.p. In C) Example NHz SCH, 2-CH3 4-CI 6-CH, 3-CI H m.p.
Amorphous. 1 Anal. Calcd.
for C19H17N30SC12:

C, 56.16; H, 4.21; N, 10.34. Found:
C, 55.93; H, 4.21;
N, 10.01 NHz SCH3 2-CH3 4-CH3 6-CH3 3-CI H m.p.163-165 NHS SCH, 2-CH3 4-CH3 6-CH3 3-CH, H m.p.124-127 ~ 1 w NH2 SCH3 2-CH3 4-CH3 6-CH3 3-CF3 H m.p.143-146 1 'i NHz SCH, 2-CH, 4-Br 6-CH, 3-CF3 H m.p.
Amorphous. 1 Anal. Calcd.
for C20H17N30SBrF3:

C, 49.69; H) 3.53; N, 8.67. Found:
C) 49.45; H, 3.49;
N, 8.37 NHZ SCH, 2-CI 4-CF3 6-CI 2-CH3 3-CH3 m.p.196-198 Process R, RZ R" R,4 R,5 R" R,z Physical Data of (m.p. in C) Example NHz SCH, 2-CH, 4-Br 6-CH3 3-CI H m.p.
Amotphous. 1 Anal. Calcd. for C19H17N30SBrCl:
C) 50.63; H, 3.80;
N, 9.32. Found: C, 50.40; H, 3.77;
N, 8.94 N

N

J
NHz SCH, 2-CI 4-CF3 6-CI 2-CH, 5-(CH~)3 m.p.
Amorphous. 1 COzCH3 Anai. Calcd. for C24H22N3O3SCI2F3:

C, 51.43; H, 3.96;
N, 7.50. Found: C, o 51.59; H, 4.10;
N, 7.17 NHz SCH3 2-CH, 6-CH, 4-Br 2-CH3 5-CH3 m.p.
Amorphous. 1 Anal. Calcd. for ~'21 H~2NJOCJ:
C, 56.76; H, 4.99;
N, 9.45. Found: C, 56.37; H, 5.01;
N, 9.04 NHZ SCH3 2-C) 4-CF3 6-CI 2-OCH3 H m.p.172-174 . 1 Process i Rz R,3 R" R,5 R" R,Z Physical Data of R, (m.p. in C) Example NHZ OCH, 2-CI 4-CI 6-CI 2-CI H m.p.
Amorphous. 7 ' H-NMR(CDCI,):3.68 (3H) s), 5.86(2H, broad s)) 7.26-7.44(4H, m) 7.51 y (2H, s). o N

NH2 OCH2CH3 2-CI 4-CI 6-CI 2-CI H m.p.
Amorphous. 7 Anal. Calcd. for C18H13N3O2CI4:
C) 48.5?; H ) 2.94; ~
N ) w ~o 9.44. Found: C, ;

48.41; H, 2.52;
N) 9.43 0 N(CH3)z OCH3 2-CI 4-CI 6-CI 2-CI H m.p.
Amorphous. 8 HRMS for C19H15N3O2CI4:

Calcd: 456.9913 Found: 456.9960 NHZ OCH2CH3 2-CI 4-CF3 6-CI 3-CF3 5-CF3 m.p.
Amorphous. 1 Anal. Calcd. for , C20H10N30SCI2F9:

C, 41.25; H) 1.73;
N, 7.21. Found: C, 41.49; H, 2.01;
N, 7.0t Process R, R~ R" R,4 R,5 R" R,I Physical Data of (m.p. in C) Example NHS OCHzCH, 2-CI 4-CF3 6-CI 2-CH, 5-CH3 m.p.
Amorphous. 1 High Resolution Mass Spectrum Caicd. for C22H20N30CI2F3:

472.0808. Found, 472.0817 NH2 CHzCH2 2-CI 4-CF3 6-CI 2-CH3 5-CH3 m.p.
Amorphous. 6 CH High Resolution Mass Spectrum Calcd. for , Cz, HzN3~C, zFa~

469.0935. Found:

469.0889 NHS CHzCHz- 2-CI 4-CI 6-CI. 2-CH, 5-CH3 m.p.
Amorphous. 6 CH, High Resolution Mass Spectrum Calcd. for C22H20N30CI2F3:

436.0761. Found:

436.0764 Process i R, Rz R" R,4 R,5 R" R,2 Physical Data of (m.p. In C) Example NHZ SCH3 2-CI 4-CF3 6-CI 3-OCH3 H m.p.
Amorphous. 3 'H-NMR(CDCI,) d 2.38(3H) s)) 3.90(3H) s), 5.79(2H) broad s)) 7.07(1 H, d, J=7), 7.16(1 H, s), 7.23(1 H, d, J=7), 7.39(1 H, t, 7.79(2H
J=7) s) , ) W
NHz SCH3 2-CI 4-CF3 6-C1 2-CH, 5-(CH2)40Hm.p.
Amorphous. i2 ' High Resolution t ,, Mass Spectrum ' ' Calcd, for . 532.0840. Found:

532.0871 NH2 CH2CH3 2-CI 4-CF, 6-CI 2-CH3 5-CH3 m.p.
Amorphous. 6 Anal. Calcd.
for C21 H18N30CI2F3:

C, 55.29; H, 3.97; N, 8.21. Found:
C) 55.62; H, 4.35;
N, 8.15 Process R, Rz R, 3 R, 4 R, 5 R" R, Z Physical Data of (m.p. in C) Example I NHz CH2CH3 2-CI 4-CI 6-CI 2-CH3 5-CH3 m.p.
Amorphous. 6 Anal. Caicd.
for C20H18N30CI3:
C, 56.81; H) 4.29;
N, 9.94. Found:
C, 56.88; H, 4.09;
N, 9.62 o NHS SCH3 2-CI 4-CF3 6-CI 2-CF3 5-CF3 m.p.
Amorphous. 1 Anal. Calcd.
for C20H20N30SCI2F9:

C)41.25; H,1.71; , N) 7.21. Found:
C) 41.20; H, 1.87;
N, 6.89 NHz SCH3 2-CI 4-CF3 6-CI 2-CH3 5-CH2COz m.p.
Amorphous. 1 C2H5 Anai. Caicd.
for C, 50.55; H, 3.68;

N, 7.69. Found:
C, 50.50; H) 3.50;
N, 7.29 Process R) Rz R,3 R,4 R,6 R" R,z Physical Data of (m.p. in C) Example NHz SCH3 2-CI 4-CF, 6-CI 2-CH, 5-(CHz)zOHm.p.
Amorphous. 12 HRMS for -Calcd: b03.0646 Found: 503.0147 NHz SCH, 2-CI 4-CF3 6-CI 2-OCH3 5-OCH, m.p.
Amorphous. 1 'H-NMR(CDCI3) d 2.30(3H, s), 3.60(6H,s), 6.85(2H, broad s), 6.80-6.96(3H) m), 7.74(2H, s).

NHZ OCH~CH, 2-CI 4-CF3 6-CI 3-CF, H m.p.112-114 NH2 OCHzCH3 2-CI 4-CF, 6-C~ 3-CF3 H m.p.77-78 NHz OCH~CH3 2-CI 4-CF, 6-CI 3-CH, H m.p.103-104 NHz OCHzCH3 2-CH3 4-Br 6-CH, 3-CF3 H ~ m.p.158-NHS SCH3 2-CI 4-CF, 6-CI 2-CH3 5-isopropylm.p.
Amorphous. 1 - Anal.
Calcd.
for C22H20N30SCI2F'3:

- C, 52.59; H) 3.98; N, . 8.36. Found:
C, 52.39; H, 4.01;
N, 8.08 Process R, Rz R,3 R,~ R,5 R" R,~ Physical Data of (m.p. in C) Example NH2 SCH, 2-CI 4-CF3 6-CI 2-CH3 5-(CHz)30Hm.p.
Amorphous. 12 Anal. Calcd. for C22H20N3O2SCI2F3:

C, 50.97; H, 3.88;
N, 8.10. Found: C, 51.10; H, 3.96;
N, 7.60 _--- _ _.

NHz SCH3 2-CI 4-CF3 6-CI 2-COOC~HS H m.p.211-216 NHz SCH, 2-CI 4-CF3 6-CI R" and R,2 H m.p. 115-118 1 , with the phenyl to which they are attached form 1-naphthyl NHS SCH3 2-CI 4-CF, 6-CI 3-Br H m.p.
Amorphous. 1 Calcd. for C18H11 N30SBrC12F3 C41.16,H2.11,N

8.00.

Found C 41.37, H

1.92, N 7.85.

NH2 SCH3 2-CI 4-SO~ 6-CI 3-CF3 H , m.p.272-NHz Process R, R2 R" R" R,6 R" R,2 physical Data of (m.p. In C) Example NHz SCH3 2-CI 4-CF3 6-CI 3-S02NHz H m.p.99-100 1 , NH2 SCH3 2-CH, 4-Br 6-CH3 3-SOZNHZ H m.p.242-24-NHS SCH3 2-CI 4-CF3 6-CI 3-SOZN(CH3)zH m.p.
Amorphous. 1 Anal. Caicd.
for 3/1/4C4H100:
C, 44.10; H, 3.44;
N, 9.80. Found:
C, 43.88; H, 3.29;
N, 9.68 w ' i o NHz SCH3 2-CH3 4-Br 6-CH3 3-SOZN(CH3)2H m.p.
Amorphous. 1 0 Anal. Caicd.
for C21 H23N4O3S28r:

C, 48.18; H, 4.43; N, 10.70. Found:
C, 48.42; H, 4.24;
N) 10.52 NHz SCH3 2-CI 4-CF3 6-CI 3-SOzN(CH3)ZH m.p.192-NHz SCH3 2-CI 4-C) 6-C) 2-(2-thienyi)H m.p. t 71.5-172.5'1 NHz SCH, 2-CI 6-CI 4-CF3 H H m.p.192-194 NHz CH, 2-CI 6-CI 4-CF3 2-CH3 5-CH, m.p.175-176 NHS CH3 2-CH3 6-CH3 4-Br 2-CH3 5-CH3 m.p.158-160 ii Process R,~ R~ R,3 R,4 R,5 R" R,2 Physical Data of (m.p. in C) Example NHz SCH, 2-CI 6-CI 4-CF3 3-N(CH3)z H HRMS for C2o11mON4SCizF3 Calcd: 488.0452 Found: 488.0408 NH(C3H~) SCH3 2-CI 6-CI 4-CI 2-CI H Calcd. C, 49.10;5 H, 3.50; N, 8.54;

Found: C) 5o.37;
H, 3.28; N, 8.47.

N

H

NHz SOzCH3 2-CI 6-CI 4-CF3 2-CH3 5-CH3 m.p.193.5-194.5 13 NH SCH 2-CI 6-CI 4-CF3 3-phenyl H m.p.124-127 NHz SCH3 2-Ci 6-CI 4-CF3 2-pyrrolyl H HRMS Calcd.

510.0295 Found 510.0455 N(CH3)(CzHS) SCH, 2-CI 6-CI 4-CI 2-CI H FAB Mass Spectrum: 490 NHS SCH, 2-CI 6-CI 4-CI 2-CH, 5-iPr HRMS Calcd.

467.0393 Found 457.0395 NH2 SCH, 2-CI 6-CI 4-CF3 2-CH3 5-n-butyl HRMS
Cal,cd. 1 515.0809 Found 515.0892 ' Process R, R~ R,3 R,4 R,5 R" R,Z Physical Data of (m.p. in C) Example N(CzH5)2 SCH, 2-CI 6-CI 4-CF, 2-CH, 5-iPr HRMS Calcd.

657.127y Found 557.1287 NHz CH3 2-CI 6-CI 4-CI 2-CH3 5-iPr HRMS Calcd.

435.066 Found 435.0682 N(CzHS)(C3H,) SCH3 2-CI 6-CI 4-CF, 2-CH, 5-iPr MS parent 571, 5 529, 494, 360, 160 (10096) N(CzHS) (sec- SCH3 2-CI 6-CI 4-CF3 2-CH3 5-iPr HRMS Caicd.
5 i butyl) 585.1589 Found 585.1500 N(CH3)(CZH5) SCH3 2-CI 6-CI 4-CF3 2-CH3 5-iPr HRMS Calcd.

543.1121 Found 543.1166 N(CzHS)(C3H,) SCH3 2-CI 6-CI 4-CF3 2-CH3 5-iPr HRMS Calcd.

569.1277 Found 569.1433 NHz SCH, 2-CI 6-CI 4-CF, 2-n-propyl 5-CH3 HRMS Calcd.

501.os53 Found 501.0551 Process R, a R, 4 R, s R" R, z Physical Data of (m.p. in C) Example NHz SCH3 2-CI 4-CF3 6-CI 2-Br 5-Br m.p.172-174 NHZ SCH3 2-CH3 4-Br 6-CH3 2-Br 5-Br m.p.179-181 NHZ SCH3 2-CH, 4-CH3 6-CH3 2-Br 5-Br m.p.195-197 NHZ SCH3 2-CH, 4-Br 6-CH3 2-CH3 5-N02 m.p.118-119 NH2 SCH3 2-CI 4-CI 6-CI 2-C~HS H m.p.146-150 NHZ SCH3 2-CI 4-CI 6-CI 2-CF3 H .p. 175-177 m NHZ SCH3 2-CI 4-CF3 6-CI 2-CI 5-NOZ m.p.98.0-98.5 1 NHZ SCH3 2-CH3 4-Br 6-CH3 2-CI 5-NO~ m.p.116-118 NHZ SCH3 2-CI 4-CF3 6-CI 2-CH3 5-NO~ m.p.99-100 NHZ SCH3 2-CH, 4-CH3 6-CH3 2-CH3 5-NOz ~ m.p.193-NH2 SCH3 2-CI 4-CI 6-Cl 2-OC3H, H 'H-NMR
(CDCI,) 1 d o.87 (3N, t, J=7), 1.68(2H, m)) 2.32(3H, s), 3.96(2H, q) J=7), 5.80 (1 H) broad s), 6.93 (1 H~

d) J=7), 7.03 1 H, t, J=7), 7.27 (1 H, d, J=7), 7.42 (1 H, t, J=7), 7.52 (2H, s) 0=C SCH3 N
1o H2N N/
Ra Phys. Data Process of R3 RQ (m.p. in C) Example 15 CZH5CHC4H9 2,6-CI2-4-CF3Ph HRMS Calcd. 1 467.0809.

Found 467.0913.

C3H,CH=CH-CZHS 2,6-CIZ-4-CF3Ph FAB Mass 1 Spectrum:

20 2-methylcyclopentyl2,4,6-CI3Ph HRMS Calcd. 1 417.0236.

Found -417.0328.

2-OCzHS-1-naphthyi2,6-CIZ-4-CF3Ph m.p.149-151 1 2-OC2H5-1-naphthy)2,4,6-CI3 Ph m.p. 125-128 1 25 3_CF3-Ph 1,3-(CH3)2-4-NOZ-Calcd. for pyrazol-5-yl C"H,503NBSF,:

C, 46.36;
H, 3.43; N, 19.08.

Found: C, 46.51; H, 3.37;

N) 18.10.

Example 15 A. 3-Trifluoromethylphenyithioacetonitrile.
To sodium (0.62 g, 27.0 mmol) dissolved in 40 mL of ethanol was added 4.79 g (26.9 mmol) of 3-trrfiuoromethytthiophenol and 2.04 g (27.0 mmol) of chloroacetonitrile. The reaction mixture was heated at reflux for 1 hour and then stin-ed overnight at room temperature. To the cooled reaction mixture was added one volume of ether and the precipitated solids were removed by filtration. The filtrate was evaporated on the rotary evaporator to give the product as an oil in essentially quantitative yield. This material was used in the following reaction without further purification.
B. 3-Trifluoromethylphenylcyanomethyisulfoxide.
A solution of 3.00 g (13.8 mmol) of 3-trifluoromethylphenylthioacetonitrile in mL of methylene chloride was cooled to 5 ° C under dry NZ and treated with 4.89 g (28.35 mmol) of m-chloroperbenzoic acid. The reaction mixture was stirred for hours at room temperature and then cooled in ice, after which the insolubles were removed by filtration. The filtrate was washed with 10~°sodium sulfate solution until all traces of peroxides had been removed and then dried over magnesium sulfate and evaporated to a pale yellow oil which was used in the subsequent reaction without further purification.
C. 3.3-Bis-methyfthio-2-(3-tr'rfiuoromethylphenylsulfonyl)acrylonitrile.
A solution of 13.82 mmol (crude product) of 3-trifluoromethyiphenyicyanomethylsulfoxide in 30 mL of dry dimethylsutfoxide and 1.25 mL (1.58 g, 20.7 mmol) of CSz was cooled to about 15 ° C in an ice bath under dry nitrogen. Then 0.99 g (41.5 mmol) of oil-free sodium hydride was added portionwise below 20 ° C and the deep red solution was let stir at room temperature for 75 minutes. The reaction mixture was cooled to 15 ° C, quenched with 2.58 mL (5.89 g, 41.5 mmol) of methyl iodide and let stir overnight at room temperature. The reaction mixture was poured into ice/water and let granulate for 3.5 hours. The product was filtered and air dried to give 3.51 g (72%) of the product. The analytical sample was crystallized from EtOH/HZO, m.p. 109-110°C.

D. 5-Amino-1-(2,6-dichloro-4-trifluorometh~lphenyl)-4-(3-trifluoromethylbenzenesulfon~ -3-met(~Ithiopyrazole.
A suspension of 0.50 g (1.42 mmol) of 3,3-bis-methylthio-2-(3-trifiuoromethyiphenylsulfonyl)acrylonitrile and 0.35 g (1.42 mmol) of 2,6-dichloro-4-trifiuoromethylphenylhydrazine in 10 mL of ethanol was heated at refiux for 2.5 hours, solution occurring as the reaction mixture was warmed. The mixture was stirred overnight at room temperature and was then poured into cold water. The product was extracted into ethyl acetate and the extracts were dried with magnesium sulfate and evaporated. The residues were crystallized from ether, and the product was filtered off and air dried to give 314 mg (40°.6) of the desired product, m.p. 201 -203°C. Anal. Calcd. for C,eH"OZN3SZClZFe: C, 39.28; H, 2.02; N, 7.64.
Found: C, 39.35; H, 2.19; N, 7.48.
E. 5-Dimethylamino-1-12.6-dichloro-4-trifluorometh~rlphenyll-4-~benzenesulfonyl)-3-meth5rlthioayrazole.
A solution of 0.241 g (0.5 mmol) of 5-amino-1-(2,6-dichloro-4-trifiuoromethylphenyl)-4-(benzenesulfonyl)-3-methylthiopyrazole in 5 mL of dry dimethylsulfoxide was treated with 36 mg (1.5 mmol) of oil-free sodium hydride under dry nitrogen in a flame-dried flask at room temperature. After 30 minutes, a clear, pale yellow solution had formed. This solution was treated with 0.5 mL (8.0 mmoi) of methyl iodide and stirred for 1 hour. Then the reaction mixture was poured into water and extracted twice with ethyl acetate. The combined extracts were dried with brine and with magnesium sulfate and evaporated. The residues crystallized from ether to give the desired product in 819'° yield, m.p. 163 - 164°C.
Example 16 ' The foNowing compounds were prepared in accordance with Example 15.

I IN
~N~

- -R,3,R,4,R,5 R, M.P. (C) or Analysis H 2,4,6-trichloroNHZ 161-162 H 2,4,6-trichloroN(CH3)2 200-202 2-(i-propyl)2,4,6-trichloroNH2 180-182 2-OCH3 2,4,6-trichforoNHZ 212-215 2-Ci 2,4,6-trichloroNHz Anal. Calcd. for C,BH"OzN3SZCl,: C, 39.60;
H, 2.39; N, 8.33. Found:
C,39.76; H, 229; N, 8.69 H 2,6-Clz-4-CF3NHz 209.5-210.5 H 2,6-C12-4-CF3N(CH3)Z 163-164 3-CF3 2,6-CIZ-4-CF3NH2 201-203 3-CF3 2,6-CIZ-4-CF,N(CH3)Z 137-138 Example 17 4-I2-Chloronhenvl)-1-12.6-dichloro-4-trifluoromethLlphenyl)-3-methylthiopyrazolo f 3.4-dl pyrimidine.
A suspension of 669 mg (1.39 mmol) of 5-amino-1-(2,6-dichloro-4 trifluoromethylphenyl)-4-(2-chlorobenzoyl}-3-methylthiopyrazole in 5 mL of formamide was heated at 150 ° C overnight. A pale yellow solid precipitated upon cooling of the reaction mixture. A total of 50 mL of water was added to the stirred suspension to complete the precipitation of the product which was filtered off and washed with water.
An inseparable trace of starting material was observed in the product by thin layer chromatography (TLC) and so the above procedure was repeated on the mixture giving a brown solid containing no trace of starting material. Trituration of this solid with methyiene chloride gave a pale yellow solution which was concentrated to give the desired product as a white crystalline solid, m.p. 156-158 ° C.
Example 18 The following compounds were prepared in accordance with Example 17.
R .~

R

R3 Rs R,3 m.p.(C) or HRMS

2-CI-Ph H CI 193-195 3-CI-Ph H CI 171-173 2-CI-Ph H CF3 156-158 2-CI-Ph OH CI 313-316 2-CI-Ph CI CI ~ 193-195 2-CI-Ph 4-ethoxycarbonyl-CI 222-225 piperazinyl 1-naphthyl H CF3 171-173 2-CI-Ph CH, Cl 210-212 2-CH3_5-iPrPhCH3 CI 141-142 R3 R9 R,3 m.p.(C) or Hi~MS

2,6-(CH,)Z CH3 CI HRMS Calcd. 462.0239.
Ph Found, 462.0369.

2-(OCzHs)-Ph CH, CI 189.192 2-(OCZH5)-1- CH, CI HRMS: Calcd.: 528.0345 naphthyi Found: 528.0226 2-OCH3-Ph CH3 C1 214-216 2-CzH5 Ph CH3 CI HRMS: Calcd. 462.0239 Found: 462.0219 Ph CH3 CF3 114-116 2,5-(CH3)Z-PhCH3 CF3 HRMS: Calcd. 497.0579 Found: 497.0602 2-CF3-Ph CH3 CI HRMS: Caicd. 501.9800 Found: 501.9778

Claims (8)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:

1. A compound of the formula:
(wherein:
A and R1 together with the carbons to which they are attached form pyrimidinyl or 5-pyridyl, each of which may be substituted by R5 which is hydrogen, C1-C6 alkyl, fluoro, chloro, bromo, hydroxyl, amino, O(C1-C6 alkyl), NH(C1-C6 alkyl), N(C1-C6 alkyl)(C1-C6 alkyl), 4-ethoxycarbonylpiperazinyl, SH or S(O)n(C1-C6 alkyl) (in which n=0, 1 or 2), wherein each C1-C6 alkyl may contain from one to two double or triple bonds and may be substituted by from 1 to 3 substituents R6 which are independently selected from the group consisting of hydroxyl, amino, C1-C3 alkoxy, dimethylamino, diethylamino, methylamino, ethylamino, NH(C=O)CH3, fluoro, chloro, bromo and C1-C3 alkylthio;
R2 is hydrogen, C1-C6 alkyl, hydroxyl, amino, O(C1-C6 alkyl), NH(C1-C6 alkyl), N(C1-C6 alkyl)(C1-C6 alkyl), SH, S(O)n(C1-C6 alkyl) (in which n=0, 1 or 2), cyano, hydroxyl, carboxyl or amido, wherein each alkyl may be substituted by one to three substituents each independently selected from the group consisting of hydroxyl, amino, carboxyl, amido, NH(C=O)(C1-C6 alkyl), N(C1-C6 alkyl)(C1-C6 alkyl), (C=0)O(C1-C6 alkyl), C1-C3 alkoxy, C1-C3 alkylthio, fluoro, bromo, chloro, iodo, cyano and nitro;
R3 is phenyl, naphthyl, thienyl, benzothienyl, pyridyl, quinolyl, pyrazinolyl, pyrimidyl, imidazolyl, furanyl, benzofuranyl, benzothiazolyl, isothiazolyl, benzoisothiazolyl, thiazolyl, isoxazolyl, benzisoxazolyl, benzimidazolyl, triazolyl, pyrazolyl, pyrrolyl, indolyl, azaindolyl, benzoxazolyl, oxazolyl, pyrrolidinyl, thiazolidinyl, morpholinyl, pyridinyl, tetrazolyl, or 3 to 8-membered cycloalkyl or 9 to 12-membered bicycloalkyl, optionally containing one to three of O, S or N-Z (wherein Z is hydrogen, C1-C4 alkyl, C1-C4 alkanoyl, phenyl or phenylmethyl), wherein each one of the above groups may be substituted by one to three substituents each independently selected from the group consisting of fluoro, chloro, bromo, trifluoromethyl, C1-C6 alkyl and C1-C6 alkoxy, or by one of cyano, nitro, amino, NH(C1-C6 alkyl), N(C1-C4 alkyl)(C1-C2 alkyl), COO(C1-C4 alkyl), CO(C1-C4 alkyl), SO2NH(C1-C4 alkyl), SO2N(C1-C4 alkyl)(C1-C2 alkyl), SO2NH2, NHSO2(C1-C4 alkyl), S(C1-C6 alkyl) and SO2(C1-C6 alkyl), wherein each C1-C4 alkyl and each C1-C6 alkyl may be substituted by one or two substituents each independently selected from the group consisting of fluoro, chloro, hydroxyl, amino, methylamino, dimethylamino and acetyl; and R4 is phenyl, naphthyl, thienyl, benzothienyl, pryidyl, quinolyl, pyrazinolyl, pyrimidyl, imidazolyl, furanyl, benzofuranyl, benzothiazolyl, isothiazolyl, benzoisothiazolyl, thiazolyl, isoxazolyl, benzisoxazolyl, benzimidazolyl, triazolyl, pyrazolyl, pyrrolyl, indolyl, azaindolyl, benzoxazolyl, oxazolyl, pyrrolidinyl, thiazolidinyl, morpholinyl, pyridinyl, tetrazolyl, or 9 to 12-membered bicycloalkyl, optionally containing one to three of O, S or N-Z (wherein Z is hydrogen, C1-C4 alkyl, C1-C4 alkanoyl, phenyl or phenylmethyl), wherein each of the above groups may be substituted by one to three substituents each independently selected from the group consisting of fluoro, chloro, bromo, trifluoromethyl, C1-C6 alkyl and C1-C6 alkoxy, or by one of cyano, nitro, amino, NH(C1-C6 alkyl), N(C1-C4 alkyl)(C1-C2 alkyl), COO(C1-C4 alkyl), CO(C1-C4 alkyl), SO2NH(C1-C4 alkyl), SO2N(C1-C4 alkyl)(C1-C2 alkyl), SO2NH2, NH2SO2(C1-C4 alkyl), S(C1-C6 alkyl) and SO2(C1-C6 alkyl), wherein each C1-C4 alkyl and each C1-C6 alkyl may be substituted by one or two substituents each independently selected from the group consisting of fluoro, chloro, hydroxyl, amino, methylamino, dimethylamino and acetyl;
provided that R4 is not unsubstituted phenyl), or a pharmaceutically acceptable acid addition salt thereof.

2. The compound or salt according to claim 1, wherein R3 is phenyl substituted with one or two substituents each independently selected from the group consisting of fluoro, chloro, bromo, methyl, trifluoromethyl, nitro, C1-C6 alkyl, C1-C6 alkoxy, SO2NH2, SO2NH(C1-C6 alkyl), SO2N(C1-C6 alkyl)2.

3. The compound or salt according to claim 1 or 2, wherein R4 is 2,4,6-trichlorophenyl, 2,4,6-trimethylphenyl, 2,6-dichloro-4-trifluoromethylphenyl or 4-bromo-2,6-dimethyl-phenyl.

4. The compound or salt according to any one of claims 1 to 3, wherein R2 is methylthio or ethyl.

5. The compound or salt according to any one of claims 1 to 4, wherein A and R1 together form a pyrimidine ring, such that the bicyclic structure formed is pyrazolo[3,4-d]pyrimidine, and R5 is substituted at the 6 position.

6. The compound or salt according to claim 1, wherein the compound has the formula:
wherein:
R3 is as defined in claim 1;
R9 is H, OH, Cl, CH3 or 4-ethoxycarbonylpiperazinyl;
R13 is Cl or CF3.

7. The compound or salt according to claim 6, wherein R3 is 2-chlorophenyl, 3-chlorophenyl, 1-naphthyl, 2-methyl-5-isopropylphenyl, 2,6-dimethylphenyl, 2-ethoxyphenyl, 2-ethoxy-1-naphthyl, 2-methoxyphenyl, phenyl, 2,5-dimethylphenyl or 2-trifluoromethylphenyl.

8. A composition for the treatment of (a) illness induced or facilitated by corticotropin releasing factor or (b) stress-induced illness which comprises (1) an effective amount of the compound or salt of any one of claims 1 to 7 and (2) a pharmaceutically acceptable carrier.