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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013516Generated: October 31, 2026

Methyl 4-(chlorocarbonyl)benzoate → Methyl 4-[({2-[(tert-butoxycarbonyl)amino]-5-thien-2-ylphenyl}amino)carbonyl]benzoate

https://huagongshe.com/reaction/1013516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(chlorocarbonyl)benzoateHCID 81850—
Reactanttert-Butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamateHCID 57717474—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-[({2-[(tert-butoxycarbonyl)amino]-5-thien-2-ylphenyl}amino)carbonyl]benzoateHCID 57607810—

Reaction Steps

Methyl 4-(chlorocarbonyl)benzoate (0.75 g, 3.79 mmol) and anhydrous DCM (0.25 M) was treated with tert-butyl 2-amino-4-thien-2-ylphenylcarbamate (1.0 g, 3.44 mmol). The resulting solution was stirred at ambient temperature for 14 hours. The reaction mixture was quenched with a solution of aqueous NaOH (1M) and partitioned between ethyl acetate and water. The organic layer was washed with water, saturated aqueous sodium bicarbonate, brine, dried over anhydrous magnesium sulfate and then concentrated in vacuo. The residue was carried on without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981874B2
Source datasetuspto-grants-2011_07
ORD IDord-d8845d5769aa473fbb6b0accef49d1fe
Source noteuspto-grants-2011_07