GB1030030A - Derivatives of phthalimide - Google Patents
Derivatives of phthalimideInfo
- Publication number
- GB1030030A GB1030030A GB5253464A GB5253464A GB1030030A GB 1030030 A GB1030030 A GB 1030030A GB 5253464 A GB5253464 A GB 5253464A GB 5253464 A GB5253464 A GB 5253464A GB 1030030 A GB1030030 A GB 1030030A
- Authority
- GB
- United Kingdom
- Prior art keywords
- optically active
- reacting
- ethyl
- hydrogen
- acetyl
- 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
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
Abstract
Novel a - monosubstituted - a - phthalimidoacetamides of formula <FORM:1030030/C2/1> where R is ethyl, propyl or isopropyl, R1 is hydrogen, methyl, ethyl or acetyl, R2 is methyl or ethyl, and X is hydrogen or halogen, as racemates and optically active isomers, are prepared by reacting the corresponding phthalimido acid, either in optically active or inactive form, with an agent suitable for converting carboxyl groups to carboxylic acyl chloride groups, and reacting the phthalimidoacid chloride formed with ammonia or an amine HNR1R2, R1 and R2 being as defined in Claim 1 except that R1 is not acetyl, and treating, if desired, the resulting phthalimidoacetamide when R1 is hydrogen with acetic anhydride to obtain the N-acetyl derivative. The optically active phthalimidiacids can be obtained by optical resolution of the corresponding racemic acid, e.g. by fractional crystallization of its ephedrine salts, or by reacting the appropriate phthalic anhydride with an optically active a -amino-acid of formula RCH(NH2)COOH. Therapeutic compositions which are useful as tranquilizers and anticonvulsants and which may be administered orally, e.g. as tablets, pills, wafers, or cachets, contain as active ingredient the compounds described above.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5253464A GB1030030A (en) | 1964-12-28 | 1964-12-28 | Derivatives of phthalimide |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5253464A GB1030030A (en) | 1964-12-28 | 1964-12-28 | Derivatives of phthalimide |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1030030A true GB1030030A (en) | 1966-05-18 |
Family
ID=10464276
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5253464A Expired GB1030030A (en) | 1964-12-28 | 1964-12-28 | Derivatives of phthalimide |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1030030A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995001348A2 (en) * | 1993-07-02 | 1995-01-12 | Celgene Corporation | Imides as inhibitors of tnp alpha |
-
1964
- 1964-12-28 GB GB5253464A patent/GB1030030A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995001348A2 (en) * | 1993-07-02 | 1995-01-12 | Celgene Corporation | Imides as inhibitors of tnp alpha |
WO1995001348A3 (en) * | 1993-07-02 | 1995-03-09 | Celgene Corp | Imides as inhibitors of tnp alpha |
EP1477486A3 (en) * | 1993-07-02 | 2004-12-15 | Celgene Corporation | Imides as inhibitors of TNF alpha |
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