GB285873A - Process for the manufacture of higher alkylated guanidine derivatives - Google Patents
Process for the manufacture of higher alkylated guanidine derivativesInfo
- Publication number
- GB285873A GB285873A GB4800/28A GB480028A GB285873A GB 285873 A GB285873 A GB 285873A GB 4800/28 A GB4800/28 A GB 4800/28A GB 480028 A GB480028 A GB 480028A GB 285873 A GB285873 A GB 285873A
- Authority
- GB
- United Kingdom
- Prior art keywords
- guanidinopropylamine
- aminobutylaminopropylamine
- guanidinobutyl
- glyoxaline
- decamethylenediamine
- 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
- C07C277/00—Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C277/08—Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups of substituted guanidines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
285,873. Schering-Kahlbaum Akt.- Ges., (formerly Chemische Fabrik auf Actien, vorm. E. Schering). Feb. 24, 1927, [Convention date]. Addition to 279,884. Alkylguanidines are prepared by treating a salt of a higher alkylamine with cyanamide or an alkyl cyanamide in the presence of an amount of solvent which is insufficient for the formation of a solution. By this means di-isoamylamine is converted into di-isoamylguanidine, decamethylenediamine into diguanyl-decamethylenediamine, and 8-guanidinobutyl-gamma-guanidinopropylamine into the corresponding triguanidine. The Specification, as open to inspection under Sect. 91 (3) (a) also describes the conversion of methylaminoacetopyrocatechol into 2-amino-3- methyl-4 (5)-dioxyphenyl (3 : 4)-glyoxaline, and methylaminoacetophenol into 2-amino-3-methyl-4 (5)-oxyphenyl (4)-glyoxaline. This subject-matter does not appear in the Specification as accepted. #-Guanidinobutyl-gamma-guanidinopropylamine is obtained by treating aminobutylaminopropylamine with double the molecular quantity of isothiourea ether. Aminobutylaminopropylamine is prepared by interaction of putrescin with chloropropylphthalimide, followed by saponification.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE285873X | 1927-02-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB285873A true GB285873A (en) | 1929-03-21 |
Family
ID=6058941
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4800/28A Expired GB285873A (en) | 1927-02-24 | 1928-02-15 | Process for the manufacture of higher alkylated guanidine derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB285873A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2620354A (en) * | 1951-01-12 | 1952-12-02 | Int Minerals & Chem Corp | Production of guanidino fatty acids |
US2654779A (en) * | 1950-12-23 | 1953-10-06 | Int Minerals & Chem Corp | Method of preparation of guanidino fatty acids |
-
1928
- 1928-02-15 GB GB4800/28A patent/GB285873A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2654779A (en) * | 1950-12-23 | 1953-10-06 | Int Minerals & Chem Corp | Method of preparation of guanidino fatty acids |
US2620354A (en) * | 1951-01-12 | 1952-12-02 | Int Minerals & Chem Corp | Production of guanidino fatty acids |
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