HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Methyl 5-sulfamoyl-1,3-thiazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methyl 5-(chlorosulfonyl)-1,3-thiazole-4-carboxylate | HCID 15077125 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 5-sulfamoyl-1,3-thiazole-4-carboxylate | HCID 15077126 | — |
Reaction Steps
A solution of 28.9 g of methyl 5-(chlorosulfonyl)-4-thiazolecarboxylate in 150 ml tetrahydrofuran was cooled to 0° and 6.6 ml of liquid ammonia was added dropwise at 0°-10°. The suspension was allowed to warm to ambient temperature and stirred 1 hour. The reaction mixture was filtered, the ammonium chloride washed with tetrahydrofuran, and the solvent evaporated from the filtrate. The residual solid was slurried in hexane, collected and dried to give 25.0 g of the title compound, m.p. 138°-140°. IR: 3.01 and 3.1μ (SO2NH2) and 5.8μ (C=O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04919706 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-288027ee87514240a048d654d6e10fec |
| Source note | uspto-grants-1990_04 |