GB1347433A - Acetophenone oxime derivatives and pharmaceutical preparations which contain the same - Google Patents
Acetophenone oxime derivatives and pharmaceutical preparations which contain the sameInfo
- Publication number
- GB1347433A GB1347433A GB2462572A GB2462572A GB1347433A GB 1347433 A GB1347433 A GB 1347433A GB 2462572 A GB2462572 A GB 2462572A GB 2462572 A GB2462572 A GB 2462572A GB 1347433 A GB1347433 A GB 1347433A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reaction
- hydrogen
- compound
- oxime derivatives
- contain
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/15—Oximes (>C=N—O—); Hydrazines (>N—N<); Hydrazones (>N—N=) ; Imines (C—N=C)
Abstract
1347433 Acetophenone-oxime derivatives PHILIPS GLOEILAMPENFABRIEKEN NV 25 May 1972 [28 May 1971] 24625/72 Heading C2C Novel compounds I: in which Hal is bromine or chlorine and R is hydrogen or the group COR 1 where R 1 is hydrogen, C 1-11 alkyl, C 1-11 alkoxy or a group of Formula II: are prepared by (1) reaction of a 4-halogenated acetophenone with NH 2 -O-CH 2 .CH 2 -OR, (2) reaction of a compound V in which M is hydrogen or a metal with R 2 -CH 2 -CH 2 -OR in which R 2 is halogen or the tosyloxy group, (3) reaction of a compound VII: with ROH, (4) reaction of a compound I in which R is H with a compound R 3 -COR, in which R 3 is OH, halogen, C 1-4 alkoxy or R 1 -CO-O- with the proviso that when R 1 is hydrogen, R 3 is not R 1 -CO-O-, or (5) reaction of an alcohol of Formula I (R = H) with ethylene oxide. Compounds I show anti-inflammatory and analgesic activity and form with a suitable carrier a pharmaceutical preparation which may be administered orally, parenterally or rectally.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL7107360A NL7107360A (en) | 1971-05-28 | 1971-05-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1347433A true GB1347433A (en) | 1974-02-27 |
Family
ID=19813272
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2462572A Expired GB1347433A (en) | 1971-05-28 | 1972-05-25 | Acetophenone oxime derivatives and pharmaceutical preparations which contain the same |
Country Status (8)
Country | Link |
---|---|
US (1) | US3803235A (en) |
BE (1) | BE784076A (en) |
CH (3) | CH590828A5 (en) |
DE (1) | DE2225190C3 (en) |
ES (1) | ES403209A1 (en) |
FR (1) | FR2140047B1 (en) |
GB (1) | GB1347433A (en) |
NL (1) | NL7107360A (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AR205682A1 (en) * | 1970-06-11 | 1976-05-31 | Philips Nv | METHOD OF PRODUCTION OF AMINO-OXYACETIC (4-CHLORO-ALPHA-METHYLBENZYLIDEN) ESTER (2-DIMETHYLAMINOETHYL) ACID AND ITS ACID ADDITION SALTS FORMED WITH PHARMACOLOGICALLY ACCEPTABLE ACIDS |
IT1110460B (en) * | 1977-03-02 | 1985-12-23 | Ciba Geigy Ag | PRODUCTS THAT PROMOTE THE GROWTH OF PLANTS AND PRODUCTS THAT PROTECT PLANTS BASED ON BODY ETHERS AND BODY ESTERS THEIR PREPARATION AND USE |
US4581060A (en) * | 1977-03-02 | 1986-04-08 | Ciba-Geigy Corporation | Compositions, which promote plant growth and protect plants, based on oxime ethers and oxime esters |
CH632130A5 (en) * | 1977-03-02 | 1982-09-30 | Ciba Geigy Ag | Compositions on the basis of oxime ethers, oxime esters or oxime carbamates which are suitable in agriculture for crop protection |
US4353735A (en) * | 1978-08-31 | 1982-10-12 | Ciba-Geigy Corporation | Oxime derivatives for protecting plant crops |
US4488900A (en) * | 1978-08-31 | 1984-12-18 | Ciba-Geigy Corporation | Oxime derivatives for protecting plant crops |
US4488898A (en) * | 1978-08-31 | 1984-12-18 | Ciba-Geigy Corporation | Oxime derivatives for protecting plant crops |
US4488899A (en) * | 1978-08-31 | 1984-12-18 | Ciba-Geigy Corporation | Oxime derivatives for protecting plant crops |
EP1925610A1 (en) * | 2006-11-24 | 2008-05-28 | Bayer CropScience AG | Production process of 2-aminooxyethanol |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3040097A (en) * | 1959-04-06 | 1962-06-19 | Purdue Research Foundation | Beta-hydroxy alkyl ethers of oximes and production thereof |
-
1971
- 1971-05-28 NL NL7107360A patent/NL7107360A/xx not_active Application Discontinuation
-
1972
- 1972-05-23 US US00256113A patent/US3803235A/en not_active Expired - Lifetime
- 1972-05-24 DE DE2225190A patent/DE2225190C3/en not_active Expired
- 1972-05-25 CH CH770772A patent/CH590828A5/xx not_active IP Right Cessation
- 1972-05-25 CH CH1382476A patent/CH587234A5/xx not_active IP Right Cessation
- 1972-05-25 GB GB2462572A patent/GB1347433A/en not_active Expired
- 1972-05-25 CH CH1382376A patent/CH590829A5/xx not_active IP Right Cessation
- 1972-05-26 BE BE784076A patent/BE784076A/en unknown
- 1972-05-26 ES ES403209A patent/ES403209A1/en not_active Expired
- 1972-05-29 FR FR7219157A patent/FR2140047B1/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
ES403209A1 (en) | 1976-01-16 |
US3803235A (en) | 1974-04-09 |
DE2225190B2 (en) | 1980-10-16 |
DE2225190A1 (en) | 1973-01-11 |
CH590828A5 (en) | 1977-08-31 |
BE784076A (en) | 1972-11-27 |
DE2225190C3 (en) | 1982-01-21 |
NL7107360A (en) | 1972-11-30 |
CH590829A5 (en) | 1977-08-31 |
FR2140047A1 (en) | 1973-01-12 |
CH587234A5 (en) | 1977-04-29 |
FR2140047B1 (en) | 1975-06-20 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed [section 19, patents act 1949] | ||
732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
PCNP | Patent ceased through non-payment of renewal fee |