HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → 3,4-dihydro-2-methyl-3-oxo-4-(2-thiazolyl-carbamoyl)-2 H-thieno[2,3-e]1,2-thiazine 1,1-dioxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | 3,4-dihydro-4-methoxycarbonyl-2-methyl-3-oxo-2H-thieno[2,3-e] 1,2-thiazine 1,1-dioxide | HCID 16639935 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 3,4-dihydro-2-methyl-3-oxo-4-(2-thiazolyl-carbamoyl)-2 H-thieno[2,3-e]1,2-thiazine 1,1-dioxide | HCID 16639941 | — |
Reaction Steps
0.15 G. of 3,4-dihydro-4-methoxycarbonyl-2-methyl-3-oxo-2H-thieno[ 2,3-e] 1,2-thiazine 1,1-dioxide and 0.071 g. of 2-aminothiazole are dissolved in 30 ml. of absolute xylene and the solution is heated for half an hour under the reflux. After cooling, the crystals are removed by filtration, recrystallized from glacial acetic acid, and 3,4-dihydro-2-methyl-3-oxo-4-(2-thiazolyl-carbamoyl)2H-thieno[ 2,3-e] 1,2-thiazine 1,1-dioxide, melting point 236° C. to 238° C. (decomposition), is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04090020 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-a2132c149ac74cbf8bed3dce2c9cb808 |
| Source note | uspto-grants-1978_05 |