GB665675A - Process for the manufacture of derivatives of hydroxy acids - Google Patents
Process for the manufacture of derivatives of hydroxy acidsInfo
- Publication number
- GB665675A GB665675A GB31229/48A GB3122948A GB665675A GB 665675 A GB665675 A GB 665675A GB 31229/48 A GB31229/48 A GB 31229/48A GB 3122948 A GB3122948 A GB 3122948A GB 665675 A GB665675 A GB 665675A
- Authority
- GB
- United Kingdom
- Prior art keywords
- copper
- derivatives
- prepared
- salicylic acid
- salt
- 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
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/02—Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Acylamido-salicylic acids of the formula <FORM:0665675/IV (b)/1> where R1 and R2 are hydrogen or alkyl and n is an integer are prepared by treating the halogen compounds <FORM:0665675/IV (b)/2> where X is a halogen, with ammonia or primary or secondary amines. Suitable amines are ethylamine, diethylamine, isopropylamine, butylamines, amylamines, laurylamine, stearylamine and palmitylamine; when a secondary amine is used R1 and R2 may be the same or different. The halogen compounds may be the a -chloro- or bromo-acetamido, propionamido or butyramido derivatives. The reaction is preferably carried out at low temperatures to minimise hydrolysis of the acylamido group. A solvent such as alcohol may be present, together with copper, copper-bronze, or a copper salt as catalyst. The product is conveniently isolated as a salt such as the hydrochloride. The starting materials can be prepared as in Specification 664,363. Examples show the preparation of 4-glycylamido-salicylic acid and 4-diethylaminoacetamido-salicylic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB31229/48A GB665675A (en) | 1948-12-02 | 1948-12-02 | Process for the manufacture of derivatives of hydroxy acids |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB31229/48A GB665675A (en) | 1948-12-02 | 1948-12-02 | Process for the manufacture of derivatives of hydroxy acids |
Publications (1)
Publication Number | Publication Date |
---|---|
GB665675A true GB665675A (en) | 1952-01-30 |
Family
ID=10319970
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB31229/48A Expired GB665675A (en) | 1948-12-02 | 1948-12-02 | Process for the manufacture of derivatives of hydroxy acids |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB665675A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2427327A1 (en) * | 1978-06-01 | 1979-12-28 | Nitto Boseki Co Ltd | NEW L-LEUCYL-4-HYDROXYANILIDE DERIVATIVES AND THEIR APPLICATION FOR DETERMINING THE ACTIVITY OF L-LEUCIN AMINOPEPTIDASE |
FR2644697A1 (en) * | 1989-03-24 | 1990-09-28 | Poudres & Explosifs Ste Nale | ANESTHETIC COMPOUNDS WITH CONTROLLED ACTION PERIOD AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME |
-
1948
- 1948-12-02 GB GB31229/48A patent/GB665675A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2427327A1 (en) * | 1978-06-01 | 1979-12-28 | Nitto Boseki Co Ltd | NEW L-LEUCYL-4-HYDROXYANILIDE DERIVATIVES AND THEIR APPLICATION FOR DETERMINING THE ACTIVITY OF L-LEUCIN AMINOPEPTIDASE |
FR2644697A1 (en) * | 1989-03-24 | 1990-09-28 | Poudres & Explosifs Ste Nale | ANESTHETIC COMPOUNDS WITH CONTROLLED ACTION PERIOD AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME |
WO1990011292A2 (en) * | 1989-03-24 | 1990-10-04 | Societe Nationale Des Poudres Et Explosifs | Controlled-action anesthetic compounds and pharmaceutical compositions containing same |
WO1990011292A3 (en) * | 1989-03-24 | 1990-11-15 | Poudres & Explosifs Ste Nale | Controlled-action anesthetic compounds and pharmaceutical compositions containing same |
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