GB797469A - Preparation of 2-amino-5-mercapto-1, 3, 4-thiadiazoles - Google Patents
Preparation of 2-amino-5-mercapto-1, 3, 4-thiadiazolesInfo
- Publication number
- GB797469A GB797469A GB16080/56A GB1608056A GB797469A GB 797469 A GB797469 A GB 797469A GB 16080/56 A GB16080/56 A GB 16080/56A GB 1608056 A GB1608056 A GB 1608056A GB 797469 A GB797469 A GB 797469A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mercapto
- amino
- thiadiazoles
- preparation
- weight
- 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
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
- C07D285/135—Nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
2 - Amino - 5 - mercapto - 1:3:4 - thiadiazoles are prepared by the ring closure of an N:N1 - bis - (thiocarbamyl hydrazine in the presence of hydrochloric and/or hydrobromic acid and from 0.05 to 30 parts by weight (preferably 0.60 to 2.0 parts by weight) of hypophosphorous acid per 100 parts by weight of said N:N1 - bis - (thiocarbamyl) hydrazine. The hydrohalic acid may be employed as a 1 to 12 N and preferably as a 2 to 4 N solution. Reaction temperatures are preferably from 90 DEG C. to reflux. The examples describe the preparation of 2 - amino - 5 - mercapto - 1:3:4 - thiadiazole. Specifications 687,760 and 726,045 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US797469XA | 1955-10-27 | 1955-10-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB797469A true GB797469A (en) | 1958-07-02 |
Family
ID=22152543
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16080/56A Expired GB797469A (en) | 1955-10-27 | 1956-05-24 | Preparation of 2-amino-5-mercapto-1, 3, 4-thiadiazoles |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB797469A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4374993A (en) * | 1981-06-08 | 1983-02-22 | Eastman Kodak Company | Process for the preparation of the sulfate salt of 2-amino-5-alkylthio-1,3,4-thiadiazoles |
CN116063244A (en) * | 2021-11-02 | 2023-05-05 | 宁夏常晟药业有限公司 | Synthesis method of 2-amino-5-mercapto-1, 3, 4-thiadiazole |
-
1956
- 1956-05-24 GB GB16080/56A patent/GB797469A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4374993A (en) * | 1981-06-08 | 1983-02-22 | Eastman Kodak Company | Process for the preparation of the sulfate salt of 2-amino-5-alkylthio-1,3,4-thiadiazoles |
CN116063244A (en) * | 2021-11-02 | 2023-05-05 | 宁夏常晟药业有限公司 | Synthesis method of 2-amino-5-mercapto-1, 3, 4-thiadiazole |
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