GB810212A - A method for the preparation of aminoacyl anilides - Google Patents
A method for the preparation of aminoacyl anilidesInfo
- Publication number
- GB810212A GB810212A GB31665/55A GB3166555A GB810212A GB 810212 A GB810212 A GB 810212A GB 31665/55 A GB31665/55 A GB 31665/55A GB 3166555 A GB3166555 A GB 3166555A GB 810212 A GB810212 A GB 810212A
- Authority
- GB
- United Kingdom
- Prior art keywords
- betaine
- formula
- triethyl
- sodium hydroxide
- anilides
- 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
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Aminoacyl anilides of the general formula <FORM:0810212/IV (b)/1> (wherein R1, R2 and R4 are methyl or ethyl and R3 is hydrogen or methyl) are prepared by decomposing at an elevated temperature a quaternary salt which has a cation of the formula <FORM:0810212/IV (b)/2> (wherein R4 is identical with R5). This process may be combined with the formation of the starting material in situ by reacting an isocyanate of the formula <FORM:0810212/IV (b)/3> with a betaine salt having a cation of the formula <FORM:0810212/IV (b)/4> in the presence of a tertiary amine. The first of the above processes is preferably effected in presence of alkali, e.g. aqueous sodium hydroxide or sodium alcoholate, or in vacuo. In examples: (1) triethyl betaine-2 : 6-dimethylanilide-bromide is heated with sodium hydroxide solution to yield o -diethylamino-acetoxylidide-2 : 6; (2) sodium in butanol replaces the sodium hydroxide of (1); (3) triethyl betaine hydrogen sulphate and 2 : 6-dimethyl-phenyl isocyanate are refluxed in pyridine and, after removal of the pyridine, the residue is treated as in (1); (4) triethyl betaine-2 : 6-dimethylanilide-chloride is heated in vacuo to yield the product of (1). Specification 793,201 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE810212X | 1954-11-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB810212A true GB810212A (en) | 1959-03-11 |
Family
ID=6724099
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB31665/55A Expired GB810212A (en) | 1954-11-11 | 1955-11-04 | A method for the preparation of aminoacyl anilides |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB810212A (en) |
-
1955
- 1955-11-04 GB GB31665/55A patent/GB810212A/en not_active Expired
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