HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → HCID 54717107, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | HCID 54717108 | HCID 54717108 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 54717107 | HCID 54717107 | — |
Reaction Steps
0.4 g. of 6-chloro-4-hydroxy-2-methyl-3-methoxycarbonyl-2H-thieno[3,2-e]1,2-thiazine-1,1-dioxide is heated under reflux for 16 hours with 0.19 g. of 2-aminothiazole in 45 ml. of absolute xylene, while passing a stream of nitrogen through the mixture. The reaction mixture is cooled to room temperature, and the product is crystallized out by scratching and then kept overnight in the cold. The precipitate crystals are removed by filtration under suction, recrystallized from ethanol, and 6-chloro-4-hydroxy-2-methyl-3-(2-thiazolecarbamoyl)-2H-thieno[3,2-e]1,2-thiazine-1,1-dioxide having a melting point of 136°-138° (with decomposition) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04180662 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-67867f60e15e402fb94fb30741a4c97f |
| Source note | uspto-grants-1979_12 |