RU94012934A - DERIVATIVES 5-ACYLAMINO-1,2,4-TIADIAZOLES, METHOD OF THEIR RECEIVING AND CONTAINING THEIR PHARMACEUTICAL COMPOSITIONS - Google Patents
DERIVATIVES 5-ACYLAMINO-1,2,4-TIADIAZOLES, METHOD OF THEIR RECEIVING AND CONTAINING THEIR PHARMACEUTICAL COMPOSITIONSInfo
- Publication number
- RU94012934A RU94012934A RU94012934/04A RU94012934A RU94012934A RU 94012934 A RU94012934 A RU 94012934A RU 94012934/04 A RU94012934/04 A RU 94012934/04A RU 94012934 A RU94012934 A RU 94012934A RU 94012934 A RU94012934 A RU 94012934A
- Authority
- RU
- Russia
- Prior art keywords
- alkyl
- help
- tiadiazoles
- acylamino
- derivatives
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 125000004432 carbon atoms Chemical group C* 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
- HWCKGOZZJDHMNC-UHFFFAOYSA-M Tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 claims 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 238000005755 formation reaction Methods 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 1
- 150000004867 thiadiazoles Chemical class 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Claims (1)
в которой Ar обозначает ароматический азотсодержащий гетероцикл, особенно индолильный гетероцикл, замещенный или нет на азоте с помощью CO - (C1 - C4-алкила; с помощью (CH2)nCOR, в котором n обозначает 1 или 2 и R обозначает OR1 или NR2 R2 с R1 и R2, одинаковыми или разными, обозначающими водород или (С1 - С4)-алкил, с помощью гидрокси-(C1 - C4)-алкила, с помощью алкоксиалкила с 2 - 6 C-атомами, тетрагидропиранила, или с помощью цепи - (CH2)3-, последний атом углерода которой фиксирован на фенильном ядре индола с образованием шестичленного цикла, Z обозначает; (а) группу:
где A и B, независимо друг от друга, обозначают C, CH или N; и X1, X2, X3, X4, одинаковые или разные, обозначают водород, (C1 - C3)-алкил, (C1 - C3)-алкоксил, Cl, Br или трифторметил, или (б) нафтильную группу, в известных случаях замещенную; также, как к их фармацевтически приемлемым солям.The invention relates to a thiadiazole derivative of the general formula (1):
wherein Ar is an aromatic nitrogen-containing heterocycle, especially an indolyl heterocycle, substituted or not on nitrogen with CO - (C 1 - C 4 -alkyl; with (CH 2 ) n COR, in which n is 1 or 2 and R is OR 1 or NR 2 R 2 with R 1 and R 2 , the same or different, denoting hydrogen or (C 1 - C 4 ) -alkyl, with the help of hydroxy- (C 1 - C 4 ) -alkyl, with the help of alkoxyalkyl with 2 - 6 C-atoms, tetrahydropyranyl, or with the help of a chain - (CH 2 ) 3 -, the last carbon atom of which is fixed on the phenyl nucleus of indole with the formation of a six-membered cycle, Z means; (a) c upp:
where A and B, independently of one another, denote C, CH or N; and X 1 , X 2 , X 3 , X 4 , identical or different, denote hydrogen, (C 1 - C 3 ) alkyl, (C 1 - C 3 ) alkoxy, Cl, Br or trifluoromethyl, or (b) a naphthyl group, optionally substituted; as well as their pharmaceutically acceptable salts.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9304535A FR2703995B1 (en) | 1993-04-16 | 1993-04-16 | 5-ACYLAMINO 1,2,4-THIADIAZOLES, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
FR9304535 | 1993-04-16 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU94012934A true RU94012934A (en) | 1996-01-27 |
RU2129550C1 RU2129550C1 (en) | 1999-04-27 |
Family
ID=9446163
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU94012934A RU2129550C1 (en) | 1993-04-16 | 1994-04-15 | Derivatives of 5-acylamino-1,2,4-thiadiazoles, method of their synthesis and pharmaceutical composition showing affinity to cholecystokinin receptors |
Country Status (15)
Country | Link |
---|---|
US (1) | US5534530A (en) |
EP (1) | EP0620221A1 (en) |
JP (1) | JP3029372B2 (en) |
CN (1) | CN1050128C (en) |
AU (1) | AU678208B2 (en) |
CA (1) | CA2121425A1 (en) |
FI (1) | FI941776A (en) |
FR (1) | FR2703995B1 (en) |
HU (1) | HU217549B (en) |
IL (1) | IL109275A (en) |
NO (1) | NO301163B1 (en) |
NZ (1) | NZ260313A (en) |
RU (1) | RU2129550C1 (en) |
TW (1) | TW295584B (en) |
ZA (1) | ZA942577B (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IE68593B1 (en) * | 1989-12-06 | 1996-06-26 | Sanofi Sa | Heterocyclic substituted acylaminothiazoles their preparation and pharmaceutical compositions containing them |
JPH11514361A (en) * | 1995-10-16 | 1999-12-07 | 藤沢薬品工業株式会社 | Heterocyclic compounds as H + -ATPase |
NZ314105A (en) * | 1996-02-02 | 1997-12-19 | Sumitomo Pharma | Guanidine derivative substituted with a substituted indole which is peri condensed with a heterocyclic ring |
AU6659298A (en) | 1997-02-18 | 1998-09-08 | Thomas Jefferson University | Compositions that bind to pancreatic cancer cells and methods of using the same |
FR2763337B1 (en) * | 1997-05-13 | 1999-08-20 | Sanofi Sa | NOVEL TRIAZOLE DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
US6768024B1 (en) | 2000-08-04 | 2004-07-27 | Lion Bioscience Ag | Triamine derivative melanocortin receptor ligands and methods of using same |
FR2815963B1 (en) * | 2000-10-26 | 2003-02-28 | Sanofi Synthelabo | NOVEL TRIAZOLE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
KR20030042035A (en) * | 2000-10-26 | 2003-05-27 | 사노피-신델라보 | Triazole derivatives and pharmaceutical compositions comprising them |
EP1314733A1 (en) * | 2001-11-22 | 2003-05-28 | Aventis Pharma Deutschland GmbH | Indole-2-carboxamides as factor Xa inhibitors |
CA2520546A1 (en) | 2003-03-28 | 2005-02-10 | Janssen Pharmaceutica, N.V. | Benzo[1,2,5]thiadiazole compounds |
BRPI0516027A (en) * | 2004-09-24 | 2008-08-19 | Janssen Pharmaceutica Nv | sulfonamide compounds |
US20060177438A1 (en) * | 2005-02-08 | 2006-08-10 | New England Medical Center | Methods of altering absorption of hydrophobic compounds |
CN102757427A (en) * | 2012-07-09 | 2012-10-31 | 陕西科技大学 | 2-amino-5-isoindoline-1,3-dimethyl ketone1,3,4-thiadiazole and preparation method thereof |
CN103601699A (en) * | 2013-11-04 | 2014-02-26 | 南京大学 | 1,3,4-thiadiazol-2-amide derivatives and preparation method thereof |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4874864A (en) * | 1988-05-24 | 1989-10-17 | Pfizer Inc. | Benzamide protease inhibitors |
IE68593B1 (en) * | 1989-12-06 | 1996-06-26 | Sanofi Sa | Heterocyclic substituted acylaminothiazoles their preparation and pharmaceutical compositions containing them |
GB9008123D0 (en) * | 1990-04-10 | 1990-06-06 | Lilly Industries Ltd | Pharmaceutical compounds |
FR2677356B1 (en) * | 1991-06-05 | 1995-03-17 | Sanofi Sa | HETEROCYCLIC DERIVATIVES OF SUBSTITUTED ACYLAMINO-2 THIAZOLES-5, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME. |
-
1993
- 1993-04-16 FR FR9304535A patent/FR2703995B1/en not_active Expired - Fee Related
-
1994
- 1994-04-11 IL IL109275A patent/IL109275A/en not_active IP Right Cessation
- 1994-04-12 TW TW083103218A patent/TW295584B/zh active
- 1994-04-12 AU AU59450/94A patent/AU678208B2/en not_active Ceased
- 1994-04-13 US US08/226,862 patent/US5534530A/en not_active Expired - Fee Related
- 1994-04-14 EP EP94400820A patent/EP0620221A1/en not_active Withdrawn
- 1994-04-14 ZA ZA942577A patent/ZA942577B/en unknown
- 1994-04-14 NZ NZ260313A patent/NZ260313A/en unknown
- 1994-04-15 NO NO941374A patent/NO301163B1/en not_active IP Right Cessation
- 1994-04-15 CA CA002121425A patent/CA2121425A1/en not_active Abandoned
- 1994-04-15 CN CN94103587A patent/CN1050128C/en not_active Expired - Fee Related
- 1994-04-15 RU RU94012934A patent/RU2129550C1/en active
- 1994-04-15 HU HU9401092A patent/HU217549B/en not_active IP Right Cessation
- 1994-04-15 JP JP6077047A patent/JP3029372B2/en not_active Expired - Lifetime
- 1994-04-15 FI FI941776A patent/FI941776A/en unknown
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