HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → ethyl 1-{[4-(3-{[(acetyloxy)acetyl]amino}phenyl)-1,3-thiazol-2-yl]methyl}-1H-pyrazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetoxyacetyl chloride | HCID 26297 | — |
| Reactant | HCID 58127539 | HCID 58127539 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl 1-{[4-(3-{[(acetyloxy)acetyl]amino}phenyl)-1,3-thiazol-2-yl]methyl}-1H-pyrazole-4-carboxylate | HCID 66939480 | 72% |
Reaction Steps
To a solution (4 mL) of the crude compound (310 mg, 0.88 mmol) obtained in Example 26a in tetrahydrofuran were added triethylamine (0.16 mL, 1.1 mmol) and acetoxyacetylchloride (145 mg, 1.1 mmol), and the mixture was stirred at room temperature overnight. After confirmation of the termination of the reaction by TLC, the resulting salt was removed. The solvent was evaporated under reduced pressure. The resulting crude title compound was purified by column chromatography (hexane-hexane/ethyl acetate=7/3) to give the title compound (270 mg, 72% in 2 steps) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461348B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-233d28bd2c3f4d05b91b7a8a4e8c49f9 |
| Source note | uspto-grants-2013_06 |