[go: up one dir, main page]

GB1289209A - - Google Patents

Info

Publication number
GB1289209A
GB1289209A GB1289209DA GB1289209A GB 1289209 A GB1289209 A GB 1289209A GB 1289209D A GB1289209D A GB 1289209DA GB 1289209 A GB1289209 A GB 1289209A
Authority
GB
United Kingdom
Prior art keywords
formula
compound
group
carbon atoms
specified above
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed filed Critical
Publication of GB1289209A publication Critical patent/GB1289209A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/38Heterocyclic compounds having sulfur as a ring hetero atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

1289209 Spirothioxanthenes MERCK PATENT GmbH 8 Oct 1970 [15 Nov 1969] 47849/70 Heading C2C Novel compounds of Formula I in which R<SP>1</SP> is H or an alkyl group with up to 6 carbon atoms, R<SP>2</SP> is H or an alkyl group with up to 3 carbon atoms, or R<SP>1</SP> and R<SP>2</SP>, together with the nitrogen atom to which they are attached, form a morpholine ring or a pyrrolidine, piperidine or piperazine ring which may, if desired, be substituted by a methyl or ethyl group, and R<SP>3</SP> and R<SP>4</SP> are H or Cl, or a physiologically acceptable acid addition salt or quaternary ammonium salt thereof, are prepared by one of the following methods: (a) reducing an enamine of formula in which the dashed line denotes an optional bond, (b) reacting a compound of Formula IV in which Y is Cl, Br, I, OH, or a reactively esterified OH group, and R<SP>3</SP> and R<SP>4</SP> have the meanings specified above, with a base of the formula, R<SP>1</SP>R<SP>2</SP>NH, in which R<SP>1</SP> and R<SP>2</SP> have the meanings specified above, or with a reactant that yields such a base, (c) reducing a compound of formula in which the dashed line in the cyclohexane ring represents a double bond that may, if desired, be present in this position in the compound of Formula II, X is =NOH, =NR<SP>1</SP>, (H,NR<SP>2</SP>Ac<SP>1</SP>) or (H,NR<SP>1</SP>Ac<SP>2</SP>) or another group which can be converted by reduction to the group NR<SP>1</SP>R<SP>2</SP>, Ac<SP>1</SP> is an acyl radical with up to 6 carbon atoms, Ac<SP>2</SP> is an acyl radical with up to 3 carbon atoms, and R<SP>1</SP> , R<SP>2</SP>, R<SP>3</SP> and R<SP>4</SP> have the meanings specified above, (d) an organometallic compound of Formula VI in which M is-Li or MgHal, Hal is Cl, Br or I, and R<SP>3</SP> and R<SP>4</SP> have the meanings specified above, with a hydroxylamine derivative of the formula, R<SP>1</SP>R<SP>2</SP>NA, in which A is an alkoxy group having 1 to 4 carbon atoms or Hal, (e) by hydrogenolysing, hydrolysing, alcoholysing or aminolysing a compound corresponding to Formula I and in which the amino group is present in a functionally modified form, in order to liberate the amino group, and (f) by reacting a compound of formula with a thioether-bridge forming reactant in order to obtain intramolecular cyclization and, in each case, the product obtained may be converted into a salt. 21 - Chloro - spiro[cyclohexane - 1,91 - thioxanthene] - 4 - one is obtained by oxidation of 2-chlorothioxanthene to the sulphoxide which is converted successively to 9,9 - bis - (2 - cyanoethyl - 2 - chlorothioxanthioxanthene sulphoxide, 9,9 - bis - (2 - cyanoethyl) - 2 - chlorothioxanthene, hydrolysed to the dipropionic acid, esterified to the dimethyl ester which is cyclized to give 2<SP>1</SP> - chloro - spiro[cyclohexane 1,9<SP>1</SP> - thioxanthene] - 4 - one - 3 carboxylic acid methylester which is decarboxylated. Pharmaceutical compositions in conventional forms for oral or parenteral administration and having central nervous system activity, circulation influencing activity and spasmolytic and/or anti-histamine activity, comprise an above novel compound and carriers or diluents.
GB1289209D 1969-11-15 1970-10-08 Expired GB1289209A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19691957490 DE1957490A1 (en) 1969-11-15 1969-11-15 4-Amino-spiro [cyclohexane-1,9'-thioxanthene] compounds and processes for their preparation

Publications (1)

Publication Number Publication Date
GB1289209A true GB1289209A (en) 1972-09-13

Family

ID=5751176

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1289209D Expired GB1289209A (en) 1969-11-15 1970-10-08

Country Status (16)

Country Link
US (1) US3721672A (en)
AT (5) AT298488B (en)
BE (1) BE758919A (en)
CA (1) CA954133A (en)
CH (5) CH564008A5 (en)
CS (5) CS162733B2 (en)
DE (1) DE1957490A1 (en)
DK (1) DK126044B (en)
ES (1) ES385518A1 (en)
FR (1) FR2073359B1 (en)
GB (1) GB1289209A (en)
IL (1) IL35443A (en)
NL (1) NL7015562A (en)
PL (1) PL83016B1 (en)
SE (1) SE370400B (en)
ZA (1) ZA706933B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1434486A (en) * 1974-02-04 1976-05-05 Ici Ltd Thioxanthene derivatives
GB1447583A (en) * 1974-02-04 1976-08-25 Ici Ltd Xanthene derivatives
JPS54112874A (en) * 1978-02-23 1979-09-04 Yoshitomi Pharmaceut Ind Ltd Thioxanthene derivative
ATE311377T1 (en) 1996-08-26 2005-12-15 Pfizer SPIROCYCLIC DOPAMINE RECEPTOR SUBTYPE LIGANDS
US7014925B2 (en) * 2003-04-29 2006-03-21 Canon Kabushiki Kaisha Heterogeneous spiro compounds in organic light emitting device elements
US20080207738A1 (en) * 2007-02-28 2008-08-28 Cancure Laboratories, Llc Drug combinations to treat drug resistant tumors

Also Published As

Publication number Publication date
DK126044B (en) 1973-06-04
AT300802B (en) 1972-08-10
CH561199A5 (en) 1975-04-30
CH564008A5 (en) 1975-07-15
PL83016B1 (en) 1975-12-31
BE758919A (en) 1971-05-13
SE370400B (en) 1974-10-14
ZA706933B (en) 1971-07-28
NL7015562A (en) 1971-05-18
FR2073359A1 (en) 1971-10-01
CA954133A (en) 1974-09-03
AT298488B (en) 1972-05-10
US3721672A (en) 1973-03-20
DE1957490A1 (en) 1971-06-16
AT300799B (en) 1972-08-10
FR2073359B1 (en) 1974-03-22
CH561200A5 (en) 1975-04-30
IL35443A (en) 1973-07-30
IL35443A0 (en) 1970-12-24
AT300801B (en) 1972-08-10
CS162732B2 (en) 1975-07-15
CH565173A5 (en) 1975-08-15
ES385518A1 (en) 1973-08-16
CS162734B2 (en) 1975-07-15
CS162733B2 (en) 1975-07-15
CS162735B2 (en) 1975-07-15
CS162736B2 (en) 1975-07-15
AT300803B (en) 1972-08-10
CH561201A5 (en) 1975-04-30

Similar Documents

Publication Publication Date Title
GB1467471A (en) Derivatives of 1,3-disubstituted-2,4-quinazolinediones
GB1432576A (en) Substituted phenylacetic acids
US3840546A (en) Amino derivatives of pyrazolopyridine carboxamides
GB1465826A (en) Indolypiperidyl-butyrophenones and indolyl-1,2,5,6-tetrahdro pyridyl-butyrophenones
DE69223827D1 (en) Glycyrrhetic acid derivatives
GB1301224A (en)
GB1289209A (en)
GB1373212A (en) Pyrazole compounds
US3979399A (en) Amino derivatives of pyrazolopyridine carboxamides
GB1330966A (en) N-substituted piperidine compounds methods for their production and pharmaceutical compositions containing them
IE34314L (en) Dibenzodioxocine derivatives
GB1277789A (en) Improvements in or relating to new polycyclic pyrrole derivatives
GB1417542A (en) Theophylline 7acetate salts
GB1153670A (en) Isoquinoline Derivatives and preparation thereof
GB1496491A (en) Dihydroergopeptine derivatives
GB1158868A (en) Novel 2,4-Disubstituted 7- and 8-Chloroquinolines, the preparation thereof and Compositions containing the same
GB1426200A (en) Nahpthyridine derivatives
GB1219387A (en) Bicyclo[2.2.2]oct-2-ene-amino acid compounds
GB1464431A (en) Indolobenzazepine derivatives and a process for the manufacture thereof
GB1351526A (en) Tropan-3-ol derivatives and processes for their preparation
GB1192219A (en) Improvements in or relating to Aminoalcohols and the Manufacture thereof
GB1252248A (en)
GB1384523A (en) Oxime derivatives and their preparation
GB1351754A (en) Indenopyrrole derivatives
GB1428933A (en) 5-phenyl-sulphinyl-2-benzimidazolyl-carbamic acid esters and process for their manufacture

Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PLNP Patent lapsed through nonpayment of renewal fees