GB2208648A - Sulphonyl butene derivatives and processes for their preparati - Google Patents
Sulphonyl butene derivatives and processes for their preparati Download PDFInfo
- Publication number
- GB2208648A GB2208648A GB8824140A GB8824140A GB2208648A GB 2208648 A GB2208648 A GB 2208648A GB 8824140 A GB8824140 A GB 8824140A GB 8824140 A GB8824140 A GB 8824140A GB 2208648 A GB2208648 A GB 2208648A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compound
- phenyl
- formula
- alkyl
- heterocyclic radical
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims description 9
- IPWDOHUWCJCDCV-UHFFFAOYSA-N S(=O)(=O)=C=CCC Chemical class S(=O)(=O)=C=CCC IPWDOHUWCJCDCV-UHFFFAOYSA-N 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims description 29
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
- -1 dimethylaminoethyloxy Chemical group 0.000 claims description 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004104 aryloxy group Chemical group 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- ZETIVVHRRQLWFW-UHFFFAOYSA-N 3-nitrobenzaldehyde Chemical compound [O-][N+](=O)C1=CC=CC(C=O)=C1 ZETIVVHRRQLWFW-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- WWFHKZKGZBFFBV-UHFFFAOYSA-N 1-sulfonylpropan-2-one Chemical compound CC(=O)C=S(=O)=O WWFHKZKGZBFFBV-UHFFFAOYSA-N 0.000 description 1
- WNLSVBDVIBECGA-UHFFFAOYSA-N 2-[1-(3-nitrophenyl)-3-oxobut-1-en-2-yl]sulfonylethyl pyridine-3-carboxylate Chemical compound C(C1=CN=CC=C1)(=O)OCCS(=O)(=O)C(=CC1=CC(=CC=C1)[N+](=O)[O-])C(C)=O WNLSVBDVIBECGA-UHFFFAOYSA-N 0.000 description 1
- TWMYSXRSVLFCGX-UHFFFAOYSA-N 2-[2-(dimethylamino)ethoxy]benzaldehyde Chemical compound CN(C)CCOC1=CC=CC=C1C=O TWMYSXRSVLFCGX-UHFFFAOYSA-N 0.000 description 1
- KMSPBUMYQPMCQC-UHFFFAOYSA-N 3-(benzenesulfonyl)-4-(3-nitrophenyl)but-3-en-2-one Chemical compound C=1C=CC=CC=1S(=O)(=O)C(C(=O)C)=CC1=CC=CC([N+]([O-])=O)=C1 KMSPBUMYQPMCQC-UHFFFAOYSA-N 0.000 description 1
- DJYPGILJLXDQGM-UHFFFAOYSA-N 4-(2-nitrophenyl)-3-propylsulfonylbut-3-en-2-one Chemical compound [N+](=O)([O-])C1=C(C=CC=C1)C=C(C(C)=O)S(=O)(=O)CCC DJYPGILJLXDQGM-UHFFFAOYSA-N 0.000 description 1
- OPKJBIYOZSELCA-UHFFFAOYSA-N 4-(3-nitrophenyl)but-3-en-2-one Chemical compound CC(=O)C=CC1=CC=CC([N+]([O-])=O)=C1 OPKJBIYOZSELCA-UHFFFAOYSA-N 0.000 description 1
- 208000001953 Hypotension Diseases 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 208000021822 hypotensive Diseases 0.000 description 1
- 230000001077 hypotensive effect Effects 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004344 phenylpropyl group Chemical group 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000000304 vasodilatating effect Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/80—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D211/84—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
- C07D211/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Description
9 n f-.
220864% SULPHONYL BUTENE DERIVATIVES AND PROCESSES FOR THEIR PREPARATION This invention relates to new sulphonyl butene derivatives useful as intermediates in the production of 1,4-dihydropyridine sulfone derivatives having such pharmacological activities as vasodilating, hypotensive and the like, and to processes for their preparation.
British Patent Application No. 8615240 provides compounds of the formula (1) @_ R 1 R200C so 2 R 3 H 3 c)'CH 3 H (1) in which R, is nitro or dimethylaminoethyloxy; R 2 is C l- c 6 alkyl or -(CH2)n-NR 4 RS; R 4 and R. which may be the same or different are independently hydrogen, Cl-C 6 alkyl or aralkyl; n is 1 to 6; 6 R 3 is c I- c 6 alkyl, C 2- c 6 alkenyl, phenyl or -(CH 2)n-R; 1.
0 11 R 6 is alkoxy, phenyl, aryloxy, -OC-R. or -NR,R,; R 7 is phenyl or Ncontaining heterocyclic radical; and R. and R. which may be the same or different are independently hydrogen, C,-C 6 alkyl, aralkyl or cycloalkyl, or R. and R. taken together with N-atom may form unsubstituted or substituted hereocyclic radical containing one or two N atoms, with the proviso that when R, is nitro and R 3 is CI-C 6 alkyl or phenyl, R 2 must be -(CH 2),,-NR 4 RS wherein R 4 and R. are not both alkyl and a pharmaceutically acceptable acid addition salt thereof.
That application also provides a process for preparing the compounds of formula (1) which comprises subjecting to a ring closure a compound of formula 0 so 2 R 3 H 3 d 1.11 R, (2) wherein R, and R 3 are as defined previously, and a compound of the formula H 2 NA,-,41 4 COOR (3) c i wherein R 4 is C l- c 6 alkyl and such processes wherein the compound of formula (2) is produced by reaction of a compound of formula (4) with a compound of formula (5) H 3 c 0 11 so R 2 3 (4) CHO 4_ R 1 (5) The present invention, in one aspect, provide compounds of formula (2) 0 h so 2 R 3 R 3 C^./ 0 "l (2) wherein R' is nitro or dime thylaminoe thyl oxy; R 3 is c 1_ c 6 alkyl, C 2_ c 6 alkenyl, phenyl or -(CH2)n-R 6 are intermediates useful for the synthesis of the compound of the formula (1). In the compounds of the invention, the substituent R, is in any position of ortho, meta or para relative to the phenyl nucleus, but preferably in the o- or m-position. Concrete examples of R 3 include methyl, ethyl, 1 1 n-propylr i-propyl, n-butyl, vinyl, phenyl, benzyl, phenylethyl, phenylpropyl, benzolyoxyethyl, -CH2 CH 2 -N (CH 3) -CH 2 -c - I-\ - -NI r X.. - CH -CO -CH CH -N N-CH2-C, -N(CH3)-CF-CH2 CH 2 Nxj 2 2 2 \--i and -NHCH2 CH2 The present invention further provides a process for producing the compounds of formula (2) by reacting a compound of the formula (4) with a compound of the formula (5) in accordance with the r -,-.ctictnscheme below.
0 CHO 11 S02 R E3 C 3 + 4- R, (4) (5) 0 0 2 R 3 a 3 c (2) The above reaction can be conducted in the presence or absence of a solvent, but preferably in the presence of a solvent inert to the reaction. The solvents used include hydrocarbons, e.g,. hexane, heptane, octane, ligroin, 1 benzene, toluene, xylene, halogenated hydrocarbons, e.g., dichlorethane, carbon tetrachloride.
The molar ratio of the compound of the formula (4) to the compound of the formula (5) can be varied over the broad range such as 1:10 to 10:1. The both compound are usually used in equimolecular amounts.
The reaction is usually conducted at temperatures ranging from an ordinary temperature to 1000C.
The reaction is preferably carried out in the presence of an organic base catalyst. Examples of the catalyst include pyrolidine, piperidine, morpholine and the like.
The compounds of the formula (2) as thus prepared are taken from the reaction mixtures by purification techniques such as concentration, recrystallization, chromatography and distillation.
The following examples will serve to further illustrate the nature of the present invention without being a limitation on the scope thereof, the scope being defined solely by the appended claims.
is solely by the appended claims.
EXAMPLE 1
1-(3-Nitrophenyl)-2-n-propylsulfonyl-lbuten-3-one A solution of l-n-propylsulfonyl-2-propanone(S.6 g) and m- nitrobenzaldehyde (6.85 g) in 100 ml of benzene was heated continuously under reflux for 6 hours in the presence of catalytic amount (3 drops) of piperidine, while removing azeotropically producing water with Molecular Sieve 3A. The reaction solution was concentrated and purified by silica gel chromatography to give 7.02 g (66% yield) of 1-(3-nitrophenyl)2-npropylsulfonyl-l-buten-3-one in the hexane effluent portion containing 5% ethyl acetate.
The title compound is identified below.
0 H cj--,so 2 nPr 3 -, NO 2 C'" M.P. 116.8 118.20C NMR (CDC1 3 6) 1.1 (3H, t, J=7 Ez) 1. 91 (2H, m) 2.22 (3H, s) 2.6-3.0 (2H, m) 7. 55 (1H, s) 1 k 7.61-8.32 (4H, m) The same procedure as mentioned in Example 1 was repeated by varying the starting materials to give the compounds which are listed below.
is 1) 2-Benzenesulfonyl-l-(3-nitrophenyl) buten-3-one 0 H 3 CA so 2 -c 0 0 2 Pale yellow crystal M.P. 124.6 126.51C NMR (CDC1 3 6) 2.36 (3H, s) 7.52-7.90 (8H, m) 8.20-8.32 (2H, m) IR (Nujol # cm-1) 1695, 1615, 1540 2) 2-(2-Benzoylo -ethyl IsulfofiY1-1.T XY (3-nitrophenyl)-1-buten-3-one 0 so 2,,.OC H 3 0- 2 0 Nujol is the registered Trade 4. 1 i 1 Pale yellow crystal M.P. 142.0 142.9C NMR (CDC1 3 6) 2.35 (3H, s) 3.82 (2H, t, J=6 Hz) 4.78 (2H, t, J=6 Hz) 7.26-8.30 UOH, m) IR (Nuiol, cm-1) 1720, 1685, 1625, 1540 3) 2-(2-Nicotinoyloxyethyl)sulfonyl-l- (3-nitrophenyl)-1-buten-3-one 0 H 3 c J.11, 0 vo 0 2 OCO ON NMR (CDC1 3 ' C- 2.37 (3H, s) 2.83 (2H, t, J=6 Hz) 4.83 (2H, t, J=6 HZ) 7.30-9.13 (9H, m) IR (neat, em-') 1720, 1690, 1615, 1590, 1530 MASS 404 (M), 387, 266, 106 (100%) 4) 1-(3-Nitrophenyl)-2-(3phenylpropyl)sulfonyl-l buten-3-one 1 -g- 0 H 3 c J, 0 2 NO 2 is Z1 NMR (CDC1 3' 6) 2.14 (2H, m) 2.36 (3H, S) 2.79 (2H, t, J=7 HZ) 3.27 (2H, m) 7.17-8.72 (10H, m) IR (neat, cm-1) 1700, 1615, 1530 MASS 0 374 (M++1), 309, 251, 183, 117, 91 (100%) 1-(2-Nitrophenyl)-2-n-propylsulfonyl-l- buten-3-one 0 SO nPr H C 3 0 0 2 0 1 NMR (CDC1 3' 6) 1.11 (3H, t, J=7 Hz) 1.86 (2H, m) 2.16 M, s) 3.29 (2H, m) 9 1 7.27-8.31 (4H, m) IR (neat, cm-1) 1700, 1610, 1575, 1530 6) 1-(3-Nitrophenyl)-2-(4-phenylbutyl)sulfonyl-l buten-3-one 0 E3 c 2 NO 2 0 0 NMR (CDC1 3 ' 6) 1.74-1.92 (4H, m) 2.35 (3H, S) 2.66 (2H, t, J=7 Hz) 3.29 (2H, t, J=7 HZ) 7.11-8.73 (9H, m) 10.13 (1H, S) IR (neat, cm-1) 3080, 3020, 2930, 2850, 1700, 1615 EXAMPLE 2 1-(3-Nitrophenyl)-2-n-butylsulfonyl-lbuten-3-one Following the same procedure as mentioned in Example 20 1, 0.85 9 (20.8%) of 1-(3nitrophenyl)-2-n-butylsulfonyl-lbuten-3-one was prepared as an oily substance from l-n-butyl- j! 1 1 sulfonyl-2-propanone (2.34 g) and m-nitrobenzaldehyde (2.98 g).
The title compound is identified below.
0 H 3 C.' so 2 n BU 0 _,,, N02 NMR (CDC1 3' 6) EXAMPLE 3
1-[2-(2-Dimethylaminoethyloxy)phenyll-2n-propylsulfonyl-l-buten-3-one Following the same procedure as mentioned in Example 1, 2.98 g (77.1%) of 1-[2-(2-dimethylaminoethyloxyphenyll- 2-n-propylsulfonyl-l-buten-3-one was prepared from l-n-propyl sulfonyl-2- propanone (1.87 g) and 2-(2-dimethylaminoethyloxy)benzaldehyde (2.20 g).
The title compound is identified below. 0 Al SO n Pr H 3 C., 2 0.97 (3H, t, J=7 Hz) 1.3-1.9 (4H, m) 2.26 (3H, S) 2.7-3.1 (2H, m) 7.6-8.3 (5H, m) U,t \--NMe2 0 1 NMR (CDC1 3' 6) -1.08 OH, t, J=7 HZ) 1.82 (2H, m) 2.25 OH, 5) 2.36 (6H, S) 2.78 (2H, t, J=6 HZ) 3.2-3.3 (2H, m) 4.15 (2H, t, J=6 EZ) 6.9-7.4 (4H, in) 8.04 (1H, S)
Claims (7)
1. A compound of formula (2) 0 H 3 c 0 2 R 3 1, R 1 (2) wherein Rl is nitro or dimethylaminoethyloxy; R 3 is C 1- C 6 alkyl, C 2- C 6 alkenyl, phenyl, substituted amino or -(CH 2), -R 6; 0 11 R. is alkoxy, phenyl, aryloxy, -OC-R 7 or NR, R9; R 7 is phenyl or N-containing heterocyclic radical; and R. and R 9' which may be the same or different are independently hydrogen, C1-C. alkyl, aralkyl or cycloalkyl, or R. and R 9 taken together with N-atom may form unsubstituted or substituted heterocyclic radical containing one or more two N atoms.
2. A compound of claim I wherein R, is o-nitro or m-nitro.
3. A compound of claim 1 wherein R, is dimethylaminoethyloxy.
1 n.
T I 1
4. A compound of any one of the preceding claims wherein R 3 is CI-C 6 alkyl, C -C, alkenyl, phenyl or 0 11 -(CH2)n-R6i R6 is alkoxy, phenyl, aryloxy, -OC-R7 or _NR&Rg, R7 is phenyl or N-containing heterocyclic radical, R. and R. are C,-C, alkyl, aralkyl or cycloalkyl, and R. and R. taken together with N-atom may form unsubstituted or substituted heterocyclic radical containing one or two N atoms.
5. A process for preparing a compound of the formula (2) wherein R. and R 3 are as defined in any one of claims 1 to 4 which comprises reacting a compound of the formula 0 11 so 2 R ]a 3 C,,," (4) wherein R 3 is as defined previously, with a compound of the formula CEO 0 R, 6- wherein R, is as defined previously.
6. A compound of claim 1 (5) hereinbefor e k -is- 1 1 specifically mentioned.
7. A process according to claim 5 substantially as hereinbefore described with reference to any one of the Examples.
Published 1988 at The Patent Wice. State House. 6671 High Holborn. London WC1R 4TP. Further copies may be obtained from The Patent Office.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60135990A JPS61293972A (en) | 1985-06-24 | 1985-06-24 | 1,4-dihydroxypyridinesulfone derivative and production thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| GB8824140D0 GB8824140D0 (en) | 1988-11-23 |
| GB2208648A true GB2208648A (en) | 1989-04-12 |
| GB2208648B GB2208648B (en) | 1990-03-07 |
Family
ID=15164617
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB8615240A Expired - Fee Related GB2178738B (en) | 1985-06-24 | 1986-06-23 | 1,4-dihydropyridine sulfone derivatives, processes for their preparation and pharmaceutical compositions comprising the same |
| GB8824140A Expired - Fee Related GB2208648B (en) | 1985-06-24 | 1988-10-14 | Suphonyl butene derivatives and processes for their preparation |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB8615240A Expired - Fee Related GB2178738B (en) | 1985-06-24 | 1986-06-23 | 1,4-dihydropyridine sulfone derivatives, processes for their preparation and pharmaceutical compositions comprising the same |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JPS61293972A (en) |
| DE (1) | DE3620632A1 (en) |
| FR (1) | FR2588003B1 (en) |
| GB (2) | GB2178738B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20210401992A1 (en) * | 2018-06-26 | 2021-12-30 | Tsrl, Inc. | Metabolically stable prodrugs |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2207523T3 (en) | 1999-06-14 | 2004-06-01 | Ortho-Mcneil Pharmaceutical, Inc. | DITIEPINO (6,5-b) PIRIDINE AND ASSOCIATED COMPOSITIONS AND PROCEDURES. |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2616995A1 (en) * | 1976-04-17 | 1977-10-27 | Bayer Ag | Sulphur substd. (1,4)-dihydro-pyridine derivs. - with circulatory activity, e.g. vasodilating and hypotensive effects |
| DE2639498A1 (en) * | 1976-09-02 | 1978-03-09 | Bayer Ag | NEW SULFUR-CONTAINING AMINO-DIHYDROPYRIDINES, THE PROCESS FOR THEIR MANUFACTURING AND THEIR USE AS A MEDICINAL PRODUCT |
| DE2747513A1 (en) * | 1977-10-22 | 1979-05-03 | Bayer Ag | DIHYDROPYRIDINE WITH SULFUR-CONTAINING ESTER GROUPS |
| EP0111453A1 (en) * | 1982-12-10 | 1984-06-20 | Ciba-Geigy Ag | Amide derivatives |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH607848A5 (en) * | 1974-06-04 | 1978-11-30 | Bayer Ag | |
| DE2616991A1 (en) * | 1976-04-17 | 1977-10-27 | Bayer Ag | Thio-substd. dihydro-pyridine derivs. - coronary vasodilators and antihypertensives prepd. e.g. by reacting dicarbonyl cpds. with amines and thio-substd. ketones |
| US4523847A (en) * | 1983-07-07 | 1985-06-18 | International Business Machines Corporation | Frequency modulation-polarization spectroscopy method and device for detecting spectral features |
| DE3501695A1 (en) * | 1985-01-19 | 1986-07-24 | Bayer Ag, 5090 Leverkusen | USE OF SULFONYL DIHYDROPYRIDINE AS A MEDICINAL PRODUCT FOR TREATING ASTHMA |
| ZA863578B (en) * | 1985-06-21 | 1987-02-25 | Hoffmann La Roche | Dihydropyridine derivatives |
-
1985
- 1985-06-24 JP JP60135990A patent/JPS61293972A/en active Pending
-
1986
- 1986-06-20 DE DE19863620632 patent/DE3620632A1/en not_active Ceased
- 1986-06-23 FR FR868609049A patent/FR2588003B1/en not_active Expired
- 1986-06-23 GB GB8615240A patent/GB2178738B/en not_active Expired - Fee Related
-
1988
- 1988-10-14 GB GB8824140A patent/GB2208648B/en not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2616995A1 (en) * | 1976-04-17 | 1977-10-27 | Bayer Ag | Sulphur substd. (1,4)-dihydro-pyridine derivs. - with circulatory activity, e.g. vasodilating and hypotensive effects |
| DE2639498A1 (en) * | 1976-09-02 | 1978-03-09 | Bayer Ag | NEW SULFUR-CONTAINING AMINO-DIHYDROPYRIDINES, THE PROCESS FOR THEIR MANUFACTURING AND THEIR USE AS A MEDICINAL PRODUCT |
| DE2747513A1 (en) * | 1977-10-22 | 1979-05-03 | Bayer Ag | DIHYDROPYRIDINE WITH SULFUR-CONTAINING ESTER GROUPS |
| EP0001769A1 (en) * | 1977-10-22 | 1979-05-16 | Bayer Ag | Sulfur-containing esters of 1,4-dihydropyridine carboxylic acids, their preparation and pharmaceutical use |
| EP0111453A1 (en) * | 1982-12-10 | 1984-06-20 | Ciba-Geigy Ag | Amide derivatives |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20210401992A1 (en) * | 2018-06-26 | 2021-12-30 | Tsrl, Inc. | Metabolically stable prodrugs |
| US12397058B2 (en) * | 2018-06-26 | 2025-08-26 | Tsrl, Inc. | Metabolically stable prodrugs |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2588003A1 (en) | 1987-04-03 |
| GB2178738A (en) | 1987-02-18 |
| GB2178738B (en) | 1990-02-28 |
| DE3620632A1 (en) | 1987-01-02 |
| GB8615240D0 (en) | 1986-07-30 |
| GB8824140D0 (en) | 1988-11-23 |
| FR2588003B1 (en) | 1989-09-15 |
| JPS61293972A (en) | 1986-12-24 |
| GB2208648B (en) | 1990-03-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IE850280L (en) | Asymmetrical diesters. | |
| KR920005742B1 (en) | Process for the preparation of pharmaceutically useful dihydropyridinyl dicanboxylate amide and esters | |
| GB2222828A (en) | Butynylamine derivatives | |
| CA1215978A (en) | Process for preparing 2-carbamoyloxyalkyl-1,4- dihydropyridine derivatives and intermediates useful for the process | |
| JPH026354B2 (en) | ||
| HU176897B (en) | Process for preparing 3-/cyanimino/-3-amino-propionitrile derivatives | |
| GB2208648A (en) | Sulphonyl butene derivatives and processes for their preparati | |
| US4048168A (en) | Process for preparing 1-polyhaloalkyl-3,4-dihydro-2-(1H)-quinazolinones | |
| EP0298703B1 (en) | A thiophene derivative and process for preparing the same | |
| CA1270251A (en) | 2-(heteroalkyl)-1,4-dihydropyridines, process for their preparation and pharmaceutical compositions containing them | |
| US4143047A (en) | 2-sulfinyl and 2-sulfonyl oxazoles | |
| JPS6361945B2 (en) | ||
| US6348616B1 (en) | Practical synthesis of benzoxazinones useful as HIV reverse transcriptase inhibitors | |
| FI67370C (en) | MELLAN PROTECTION FOR FRAMSTATING AV 4- (4-DISUBSTITUERADE PIPERIDINYLMETHYL) -3,3-DIPHENYL-2-PYRROLIDINONE AND FORM OF FRAMSTATING FOR MELLAN PRODUCTS | |
| JP3848382B2 (en) | Process for the preparation of 2-perfluoroalkyl-3-oxazolin-5-one | |
| EP0522956B1 (en) | Preparation of 2-(2-thienyl) ethylamine and synthesis of thieno [3,2-C] pyridine derivatives therefrom | |
| HU193785B (en) | Process for producing dihydropyridine derivatives | |
| US4927970A (en) | Substituted 3-cyclobutene-1,2-dione intermediates | |
| CA1221966A (en) | Hydroxyimino and alkoxyimino derivatives of 1,4- dihydropyridine, process for the preparation thereof and pharmaceutical compositions therefrom | |
| IL93393A (en) | Process for the preparation of omicron-carboxypyridyl and omicron-carboxyquinolyl- imidazolinones | |
| US5106846A (en) | 2,3-thiomorpholinedione-2-oxime derivatives and pharmaceutical compositions containing them | |
| MX2008000469A (en) | New pyrocatechin derivatives. | |
| US4175191A (en) | 4-Phenyl isoquinolines | |
| US3539630A (en) | Acetylated(1-adamantyloxy) alkylamine compounds | |
| JP3887682B2 (en) | Method for producing 1,2-benzisothiazolin-3-one compound |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20010623 |