HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → HCID 54684928, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | HCID 54704716 | HCID 54704716 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 54684928 | HCID 54684928 | 63% |
Reaction Steps
3.0 gm (9.7 millimols) of methyl 2,5-dihydro-4-hydroxy-5-methyl-1,2-thiazino-[5,6-b]indole-3-carboxylate-1,1-dioxide, 1.0 gm-(10 millimols) of 2-amino-thiazole and 150 ml of xylene were refluxed for 3.5 hours in a Soxhlett-apparatus filled with a 4-A-molecular sieve. The reaction mixture then was filtered and yielded 2.2 gm (63% of theory) of crystalline 2,5-dihydro-4-hydroxy-5-methyl-N-(2-thiazolyl)-1,2-thiazino[5,6-b]indole-3-carboxamide-1,1-dioxide; M.p.: 260° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04137313 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-4a7c1ef81f2846898eaab4b3ffdb1785 |
| Source note | uspto-grants-1979_01 |