RU94007350A - DERIVATIVES OF BENZOXAZINE, METHOD FOR THEIR PRODUCTION, PHARMACEUTICALS, INTERMEDIATE CONNECTION - Google Patents
DERIVATIVES OF BENZOXAZINE, METHOD FOR THEIR PRODUCTION, PHARMACEUTICALS, INTERMEDIATE CONNECTIONInfo
- Publication number
- RU94007350A RU94007350A RU94007350/04A RU94007350A RU94007350A RU 94007350 A RU94007350 A RU 94007350A RU 94007350/04 A RU94007350/04 A RU 94007350/04A RU 94007350 A RU94007350 A RU 94007350A RU 94007350 A RU94007350 A RU 94007350A
- Authority
- RU
- Russia
- Prior art keywords
- group
- tetrahydroisoquinolin
- methoxy
- phenyl
- dimethoxy
- Prior art date
Links
- 150000005130 benzoxazines Chemical class 0.000 title claims 2
- 239000003814 drug Substances 0.000 title 1
- -1 4-phenyl (piperidin-1-yl) group Chemical group 0.000 claims 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 claims 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- YZCKVEUIGOORGS-UHFFFAOYSA-N hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Claims (1)
где Y - атом водорода, фтора или хлора или метильная или метокси-группа, R1 - либо фенильная группа, замещенная атомом фтора или группой, выбранной из метильной, метокси-, трифторметильной и фенильной групп, либо тиен-2-ильная группа, R2 - метильная группа, R3 - либо (С1-С4)алкильная группа, либо фенил (С1-С2)алкильная группа, в которой кольцо, при необходимости, замещено 2-3 метокси-группами, либо 2-(пиридин-2-ил)этильная группа, или R2 и R3 образуют вместе с азотом либо 4-фенил(пиперидин-1-ильную)группу, либо 4-фенилметил(пиперидин-1-ильную)группу, либо 1,2,3,4-тетрагидроизохинолин-2-ильную группу, либо 6-метокси-1,2,3,4-тетрагидроизохинолин-2-ильную группу, либо 5,8-диметокси-1,2,3,4-тетрагидроизохинолин-2-ильную группу, либо 6,7-диметокси-1,2,3,4-тетрагидроизохинолин-2-ильную группу, либо 2,3,4,5-тетрагидро-1Н-3-бензазепин-3-ильную группу, либо 7,8-диметокси-2,3,4,5-тетрагидро-1Н-3-бензазепин-3-ильную группу, а Х - либо карбонильная группа, либо сульфонильная группа, обладают высокой фармацевтической активностью и применяются в терапии.Proposed benzoxazine derivatives of the general formula
where Y is a hydrogen, fluorine or chlorine atom or a methyl or methoxy group, R 1 is either a phenyl group substituted by a fluorine atom or a group selected from a methyl, methoxy, trifluoromethyl and phenyl groups, or a thien-2-yl group, R 2 is a methyl group, R 3 is either a (C 1 -C 4 ) alkyl group, or a phenyl (C 1 -C 2 ) alkyl group in which the ring is optionally substituted by 2-3 methoxy groups, or 2- ( a pyridin-2-yl) ethyl group, or R 2 and R 3 form together with nitrogen either a 4-phenyl (piperidin-1-yl) group, or 4-phenylmethyl (piperidin-1-yl) group, or 1,2, 3 , 4-tetrahydroisoquinolin-2-yl group, or 6-methoxy-1,2,3,4-tetrahydroisoquinolin-2-ilen group, or 5,8-dimethoxy-1,2,3,4-tetrahydroisoquinolin-2-ilen group, or 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-2-yl group, or 2,3,4,5-tetrahydro-1H-3-benzazepin-3-yl group, or 7.8 -dimethoxy-2,3,4,5-tetrahydro-1H-3-benzazepin-3-yl group, and X - either a carbonyl group or a sulfonyl group, has high pharmaceutical activity and is used in therapy.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9302659 | 1993-03-08 | ||
FR02659 | 1993-03-08 | ||
FR9302659A FR2702477B1 (en) | 1993-03-08 | 1993-03-08 | Benzoxazine derivatives, their preparation and their therapeutic application. |
Publications (2)
Publication Number | Publication Date |
---|---|
RU94007350A true RU94007350A (en) | 1995-11-10 |
RU2130020C1 RU2130020C1 (en) | 1999-05-10 |
Family
ID=9444751
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU94007350A RU2130020C1 (en) | 1993-03-08 | 1994-03-05 | Derivatives of benzoxazine, methods of their synthesis, a pharmaceutical preparation |
Country Status (20)
Country | Link |
---|---|
US (1) | US5447928A (en) |
EP (1) | EP0614893B1 (en) |
JP (1) | JPH0710852A (en) |
CN (1) | CN1099032A (en) |
AT (1) | ATE166648T1 (en) |
AU (1) | AU673226B2 (en) |
CA (1) | CA2117122A1 (en) |
CZ (1) | CZ284789B6 (en) |
DE (1) | DE69410509T2 (en) |
DK (1) | DK0614893T3 (en) |
ES (1) | ES2119099T3 (en) |
FI (1) | FI941068A (en) |
FR (1) | FR2702477B1 (en) |
HU (1) | HUT70539A (en) |
IL (1) | IL108885A (en) |
NO (1) | NO300542B1 (en) |
NZ (1) | NZ260039A (en) |
RU (1) | RU2130020C1 (en) |
SK (1) | SK27494A3 (en) |
TW (1) | TW302362B (en) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1109880A (en) * | 1994-02-03 | 1995-10-11 | 合成实验室公司 | 3-(2-aminoethyl)-4-[3-(trifluoromethyl) benzoyl]-3,4-dihydro-1,4-benzoxazine derivative and preparation of same |
US6339087B1 (en) | 1997-08-18 | 2002-01-15 | Syntex (U.S.A.) Llc | Cyclic amine derivatives-CCR-3 receptor antagonists |
IL125658A0 (en) | 1997-08-18 | 1999-04-11 | Hoffmann La Roche | Ccr-3 receptor antagonists |
WO1999038500A2 (en) * | 1998-01-30 | 1999-08-05 | The Brigham And Women's Hospital, Inc. | The human calcium-sensing receptor in the detection and treatment of cancer |
TW472491B (en) * | 1999-03-19 | 2002-01-11 | Seiko Epson Corp | Projection system and projector |
US6391907B1 (en) | 1999-05-04 | 2002-05-21 | American Home Products Corporation | Indoline derivatives |
US6509334B1 (en) | 1999-05-04 | 2003-01-21 | American Home Products Corporation | Cyclocarbamate derivatives as progesterone receptor modulators |
US6358948B1 (en) | 1999-05-04 | 2002-03-19 | American Home Products Corporation | Quinazolinone and benzoxazine derivatives as progesterone receptor modulators |
US6355648B1 (en) | 1999-05-04 | 2002-03-12 | American Home Products Corporation | Thio-oxindole derivatives |
UA73119C2 (en) | 2000-04-19 | 2005-06-15 | American Home Products Corpoir | Derivatives of cyclic thiocarbamates, pharmaceutical composition including noted derivatives of cyclic thiocarbamates and active ingredients of medicines as modulators of progesterone receptors |
AU2005292314B2 (en) * | 2004-09-29 | 2011-11-03 | Portola Pharmaceuticals, Inc. | Substituted 2H-1,3-benzoxazin-4(3H)-ones |
AR051780A1 (en) * | 2004-11-29 | 2007-02-07 | Japan Tobacco Inc | FUSIONED RING COMPOUNDS CONTAINING NITROGEN AND USING THEMSELVES |
HU230826B1 (en) | 2014-11-19 | 2018-07-30 | Richter Gedeon Nyrt. | Process for preparation of benzazepine derivatives |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1287584B (en) * | 1962-07-04 | 1969-01-23 | Thomae Gmbh Dr K | Process for the preparation of 2, 3-dihydro-1, 4-benzoxazine derivatives |
GB8803419D0 (en) * | 1988-02-15 | 1988-03-16 | Erba Carlo Spa | 1 4-benzoxazine & 1 4-benzothiazine derivatives & process for their preparation |
AU638154B2 (en) * | 1990-10-04 | 1993-06-17 | Suntory Limited | Benzoxazine derivative and herbicide containing same as an active ingredient |
DE4037427A1 (en) * | 1990-11-24 | 1992-05-27 | Kali Chemie Pharma Gmbh | HETEROCYCLICALLY SUBSTITUTED PIPERAZINOALKYLBENZAZAZINE AND -THIAZIN COMPOUNDS, AND METHOD FOR THE PRODUCTION THEREOF, AND THE MEDICAMENTS CONTAINING SUCH COMPOUNDS |
-
1993
- 1993-03-08 FR FR9302659A patent/FR2702477B1/en not_active Expired - Fee Related
-
1994
- 1994-02-23 DE DE69410509T patent/DE69410509T2/en not_active Expired - Fee Related
- 1994-02-23 EP EP94400382A patent/EP0614893B1/en not_active Expired - Lifetime
- 1994-02-23 DK DK94400382T patent/DK0614893T3/en active
- 1994-02-23 ES ES94400382T patent/ES2119099T3/en not_active Expired - Lifetime
- 1994-02-23 AT AT94400382T patent/ATE166648T1/en not_active IP Right Cessation
- 1994-02-24 US US08/201,233 patent/US5447928A/en not_active Expired - Fee Related
- 1994-03-05 RU RU94007350A patent/RU2130020C1/en active
- 1994-03-07 CN CN94102625A patent/CN1099032A/en active Pending
- 1994-03-07 TW TW083101951A patent/TW302362B/zh active
- 1994-03-07 SK SK274-94A patent/SK27494A3/en unknown
- 1994-03-07 CZ CZ94516A patent/CZ284789B6/en unknown
- 1994-03-07 JP JP6035758A patent/JPH0710852A/en active Pending
- 1994-03-07 IL IL108885A patent/IL108885A/en not_active IP Right Cessation
- 1994-03-07 FI FI941068A patent/FI941068A/en unknown
- 1994-03-07 NZ NZ260039A patent/NZ260039A/en unknown
- 1994-03-07 NO NO940788A patent/NO300542B1/en unknown
- 1994-03-07 CA CA002117122A patent/CA2117122A1/en not_active Abandoned
- 1994-03-07 AU AU57586/94A patent/AU673226B2/en not_active Ceased
- 1994-03-07 HU HU9400671A patent/HUT70539A/en unknown
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