HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromothiazole → ethyl 2-[3-fluoro-4-(N-thiazol-2-ylamino)phenyl]propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromothiazole | HCID 76430 | — |
| Reactant | Ethyl 2-(4-amino-3-fluorophenyl)propanoate | HCID 20364696 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 2-[3-fluoro-4-(N-thiazol-2-ylamino)phenyl]propionate | HCID 20364701 | 63.6% |
Reaction Steps
A mixture of ethyl 2-(3-fluoro-4-aminophenyl)propionate (15 g) and 2-bromothiazole (11.7 g) is stirred at 150°-155° C for 15 minutes. The reaction mixture is dissolved in methylene chloride and the solution is washed with an aqueous solution of sodium hydrogen carbonate and dried. The solvent is evaporated. The residue is subjected to chromatography using alumina. From benzene eluate, ethyl 2-[3-fluoro-4-(N-thiazol-2-ylamino)phenyl]propionate (13.3 g) is obtained as oily substance boiling at 162°-164° C at 0.2 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04077968 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-0e350db437c540e2907730dbbb7eeeb8 |
| Source note | uspto-grants-1978_03 |