HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiazole → benzyl N-(1,3-thiazol-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Product | benzyl N-(1,3-thiazol-2-yl)carbamate | HCID 5113639 | 70% |
Reaction Steps
To a stirred solution of 2-aminothiazole (AA1-A, 3.0 g, 30.0 mmol) and triethylamine (6.30 mL, 45.0 mmol) at 0° C. was added benzyl chloroformate (5 mL, 36 mmol). The reaction was stirred at RT O/N. The reaction mixture was washed with a saturated aqueous solution of NaHCO3, then water and concentrated to dryness under reduced pressure. The resulting yellow solid was crystallized from ethanol to afford AA1-2 in 70% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133235B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-1b383bf2754e46beb060a6433f482530 |
| Source note | uspto-grants-2015_09 |