GB1206216A - Aminopropylidene dibenzoxepine tranquilizers - Google Patents
Aminopropylidene dibenzoxepine tranquilizersInfo
- Publication number
- GB1206216A GB1206216A GB23194/68A GB2319468A GB1206216A GB 1206216 A GB1206216 A GB 1206216A GB 23194/68 A GB23194/68 A GB 23194/68A GB 2319468 A GB2319468 A GB 2319468A GB 1206216 A GB1206216 A GB 1206216A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxepine
- dihydrodibenz
- piperazino
- dibenzoxepine
- aminopropylidene
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D313/00—Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
- C07D313/02—Seven-membered rings
- C07D313/06—Seven-membered rings condensed with carbocyclic rings or ring systems
- C07D313/10—Seven-membered rings condensed with carbocyclic rings or ring systems condensed with two six-membered rings
- C07D313/12—[b,e]-condensed
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
1,206,216. Aminopropylidene dibenzoxepine compounds. CHAS. PFIZER & CO. Inc. 15 May, 1968 [18 July, 1967], No. 23194/68. Heading C2C. Novel aminopropylidene dibenzoxepine compounds of the formula and the pharmaceutically-acceptable acid addition salts thereof, where Y is -S-, -SO-, or -SO 2 -; and Z is C 1-4 alkylamino, di- (C 1-4 alkyl) amino, pyrrolidino, piperidino, homopiperidino, morpholino, thiamorpholino, piperazino, N - (C 1-4 alkyl) piperazino or N- (C 2-4 hydroxyalkyl) piperazino, are obtained by treating the appropriate 2-CF 3 Y-substituted- 6,11 - dihydrodibenz - [b,e] - oxepine - 11 - one with a phosphorane compound of the formula R 3 P = CHCH 2 CH 2 Z, where R is C 1-6 alkyl, phenyl, aminophenyl or benzyl (the phosphorane compound being generated in situ by reaction of the corresponding phosphonium halide hydrohalide salt with a strong base such as nbutyl lithium), followed optionally by conversion to the acid addition salts. The preparation of the following intermediates is described: 2 - Trichloromethylthio - 6,11 - dihydrodibenz- [b,e] - oxepine - 11 - one is obtained by chlorinating the corresponding 2-methylthio compound, and is heated with antimony trifluoride to form 2 - trifluoromethylthio - 6,11 - dihydrobenz - [b,e] - oxepine - 11 - one. This product is also formed from p-trifluoromethylthiophenol by reacting with phthalide to yield 2-(p-trifluoromethylthiophenoxymethyl) - benzoic acid which is heated with P 2 O 5 to form the dihydrobenz-[b,e]-oxepinone; this product is reacted with m-chloroperbenzoic acid to form 2-trifluoromethylsulphinyl - 6,11 - dihydrodibenz- [b,e]-oxepine- 11 -cee.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US65406967A | 1967-07-18 | 1967-07-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1206216A true GB1206216A (en) | 1970-09-23 |
Family
ID=24623323
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23194/68A Expired GB1206216A (en) | 1967-07-18 | 1968-05-15 | Aminopropylidene dibenzoxepine tranquilizers |
Country Status (2)
Country | Link |
---|---|
FR (1) | FR7617M (en) |
GB (1) | GB1206216A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7271176B2 (en) | 1998-09-04 | 2007-09-18 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists and methods of use thereof |
US7541365B2 (en) | 2001-11-21 | 2009-06-02 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists and methods of use therefor |
US7732459B2 (en) | 2002-11-13 | 2010-06-08 | Millennium Pharmaceuticals, Inc. | CCR1 antagonists and methods of use therefor |
-
1968
- 1968-05-15 GB GB23194/68A patent/GB1206216A/en not_active Expired
- 1968-05-22 FR FR152651A patent/FR7617M/fr not_active Expired
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7271176B2 (en) | 1998-09-04 | 2007-09-18 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists and methods of use thereof |
US7541365B2 (en) | 2001-11-21 | 2009-06-02 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists and methods of use therefor |
US8058287B2 (en) | 2001-11-21 | 2011-11-15 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists and methods of use therefor |
US8653096B2 (en) | 2001-11-21 | 2014-02-18 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists and methods of use thereof |
US9663537B2 (en) | 2001-11-21 | 2017-05-30 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists and methods of use |
US7732459B2 (en) | 2002-11-13 | 2010-06-08 | Millennium Pharmaceuticals, Inc. | CCR1 antagonists and methods of use therefor |
US7977350B2 (en) | 2002-11-13 | 2011-07-12 | Millennium Pharmaceuticals, Inc. | CCR1 antagonists and methods of use therefor |
US8394817B2 (en) | 2002-11-13 | 2013-03-12 | Millennium Pharmaceuticals, Inc. | CCR1 antagonists and methods of use therefor |
US9334283B2 (en) | 2002-11-13 | 2016-05-10 | Millennium Pharmaceuticals, Inc. | CCR1 antagonists and methods of use thereof |
Also Published As
Publication number | Publication date |
---|---|
FR7617M (en) | 1970-01-19 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |