HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-aminothiazole-4-carboxylate → Ethyl 2-(alpha-bromoacrylamido)thiazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-aminothiazole-4-carboxylate | HCID 73216 | — |
| Reactant | 2-Bromoacrylic acid | HCID 82633 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 2-(alpha-bromoacrylamido)thiazole-4-carboxylate | HCID 17876799 | 85.7% |
Reaction Steps
To a solution containing 0.688 g of ethyl 2-aminothiazole-4carboxilate (prepared as reported in J.A.C.S. 68,266,1946) and 0.3 g of 2-bromoacrylic acid in 10 ml of dioxane, 0.412 g of N-N'dicyclohexylcarbodiimide were and the mixture was stirred at room temperature overnight. After filtration, the solvent was evaporated in vacuo, the solid residue was dissolved in 50 ml of ethyl acetate, treated with saturated solution of sodium bicarbonate and then with 10% hydrochloric acid. The organic phase was dried over anhydrous sodium sulphate and the solvent evaporated in vacuo. The solid residue was purified by recrystallization from ethanol-water to yield 0.52 g of ethyl 2-(α-bromoacrylamido)thiazole-4-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753629 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-16b5e6a84296485abc98721cf20967e5 |
| Source note | uspto-grants-1998_05 |