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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067328Generated: November 1, 2026

Pyridine → Ethyl 3-methyl-5-(phenoxycarbonylamino)thiophene-2-carboxylate

https://huagongshe.com/reaction/2067328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
Reactant5-Amino-3-methylthiophene-2-carboxylateHCID 86645288—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-methyl-5-(phenoxycarbonylamino)thiophene-2-carboxylateHCID 4340394396%

Reaction Steps

To a stirred mixture of 5-amino-3-methylthiophene-2-carboxylate (11.87 g, 64.08 mmol) and pyridine (5.70 mL, 70.48 mml) in dichloromethane (140 mL) at 0° C. was added dropwise phenyl chloroformate (8.90 mL, 70.71 mmol). The resulting reaction mixture was stirred at ambient temperature for 30 minutes, and then quenched with water (200 mL). The aqueous layer was extracted with dichloromethane (2×200 mL), and the combined organic layer was dried over sodium sulfate, filtered and concentrated in vacuo. The residue was triturated with dichloromethane in hexanes to afford ethyl 3-methyl-5-(phenoxycarbonylamino)thiophene-2-carboxylate as a colorless solid (18.89 g, 96%): MS (ES+) m/z 306.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293768B2
Source datasetuspto-grants-2012_10
ORD IDord-45dfca6124df433cb0ccb9fa9460a106
Source noteuspto-grants-2012_10