GB1157639A - Amino-Valeramide Derivatives and Process for their Preparation - Google Patents
Amino-Valeramide Derivatives and Process for their PreparationInfo
- Publication number
- GB1157639A GB1157639A GB174769A GB174769A GB1157639A GB 1157639 A GB1157639 A GB 1157639A GB 174769 A GB174769 A GB 174769A GB 174769 A GB174769 A GB 174769A GB 1157639 A GB1157639 A GB 1157639A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- valeramide
- derivatives
- valeronitrile
- july
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1,157,639. Amino-valeramide derivatives and process for their preparation. STERLING DRUG Inc. 1 July, 1966 [1 July, 1965], No. 1747/69. Divided out of 1,157,637. Heading C2C. Compounds of the formulae may be obtained by hydrolysing 2-methyl-5- NR 1 R 2 -valeronitrile or 4 - methyl - 5 - NR 1 R 2 - valeronitrile, preferably in an aqueous mineral acid, where -NR 1 R 2 is a tertiary amino group and R 1 and R 2 are the same or different and represent lower or higher alkyl, hydroxy lower or higher alkyl, lower alkoxy higher or lower alkyl, di-lower alkylamino lower or higher alkyl, C 3-7 cycloalkyl, phenyl or substituted phenyl, said substitutents being hydroxy, lower alkoxy, di-lower alkylamino, trifluoromethyl, lower alkylmercapto or halo or R 1 and R 2 taken together form a heterocyclic ring containing at least one heteroatom, the terms " lower " and " higher " denoting C 1-8 and C 8-18 respectively. The hydrolysis is preferably effected at 60-65‹ C. in 85-95% sulphuric or phosphoric acid. The aminonitrile starting material is suitably that obtained by catalytically hydrogenating 2-methylene glutaronitrile and reductively alkylating the product in the presence of an amine, HNR 1 R 2 À
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US46895865A | 1965-07-01 | 1965-07-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1157639A true GB1157639A (en) | 1969-07-09 |
Family
ID=23861890
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB174769A Expired GB1157639A (en) | 1965-07-01 | 1966-07-01 | Amino-Valeramide Derivatives and Process for their Preparation |
GB2963666A Expired GB1157637A (en) | 1965-07-01 | 1966-07-01 | Process for the Production of Tertiary-Amino Alkylated Primary Amines |
GB174669A Expired GB1157638A (en) | 1965-07-01 | 1966-07-01 | Aminonitrile Derivatives and Process for their Preparation |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2963666A Expired GB1157637A (en) | 1965-07-01 | 1966-07-01 | Process for the Production of Tertiary-Amino Alkylated Primary Amines |
GB174669A Expired GB1157638A (en) | 1965-07-01 | 1966-07-01 | Aminonitrile Derivatives and Process for their Preparation |
Country Status (1)
Country | Link |
---|---|
GB (3) | GB1157639A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5463130A (en) * | 1994-03-07 | 1995-10-31 | Basf Aktiengesellschaft | Preparation of peralkylated amines |
US5557011A (en) * | 1992-11-26 | 1996-09-17 | Basf Aktiengesellschaft | Preparation of diamines |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4910343A (en) * | 1988-09-20 | 1990-03-20 | W. R. Grace & Co.-Conn. | Nitroamines |
DE19825452A1 (en) * | 1998-06-06 | 1999-12-09 | Basf Ag | Process for the preparation of secondary or tertiary 2-methyl-1,5-pentanediamines |
CN104803859A (en) * | 2015-04-17 | 2015-07-29 | 武汉瑞凯兴科技有限公司 | Synthetic method of 5-(N-ethyl-N-2-ethylol amine)-2-amylamine |
CN110616236B (en) * | 2019-10-14 | 2021-02-26 | 暨明医药科技(苏州)有限公司 | Preparation method of (R) -N1, N1-diethyl-1, 4-pentanediamine |
CN111253263B (en) * | 2020-02-17 | 2022-07-05 | 北京弗莱明科技有限公司 | Preparation method of chloroquine key intermediate 2-amino-5-diethylaminopentane |
-
1966
- 1966-07-01 GB GB174769A patent/GB1157639A/en not_active Expired
- 1966-07-01 GB GB2963666A patent/GB1157637A/en not_active Expired
- 1966-07-01 GB GB174669A patent/GB1157638A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5557011A (en) * | 1992-11-26 | 1996-09-17 | Basf Aktiengesellschaft | Preparation of diamines |
US5463130A (en) * | 1994-03-07 | 1995-10-31 | Basf Aktiengesellschaft | Preparation of peralkylated amines |
Also Published As
Publication number | Publication date |
---|---|
GB1157638A (en) | 1969-07-09 |
GB1157637A (en) | 1969-07-09 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |