HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 12891965, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-[(5-Nitro-1,3-benzothiazol-2(3H)-ylidene)amino]ethan-1-ol | HCID 3018769 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12891965 | HCID 12891965 | 85% |
Reaction Steps
To a stirred and cooled (0° C.) solution of 19 parts of 2-[(5-nitro-2-benzothiazolyl)amino]ethanol in 18 parts of N,N-dimethylformamide is added dropwise (slowly) a solution of 10.7 parts of thionyl chloride in 207 parts of N,N-dimethylformamide. Upon completion, the mixture is stirred and heated slowly to reflux and stirring at reflux is continued for 4 hours. After cooling, the precipitated product is filtered off and washed with N,N-dimethylformamide and 2,2'-oxybispropane, yielding 17.5 parts (85%) of 2,3-dihydro-6-nitroimidazo[2,1-b]benzothiazole monohydrochloride; mp. 314°-316° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04262004 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-e04194c65f774c9ba98088c8235bfbbe |
| Source note | uspto-grants-1981_04 |