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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746785Generated: October 30, 2026

Methyl chloroformate → HCID 59446938, compound

https://huagongshe.com/reaction/1746785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantTriethylamineHCID 8471—
ReactantHCID 59446860HCID 59446860—
Reactant6-[(Cyclopropylmethyl)(propyl)amino]pyrimidine-4-carboxylic acidHCID 59447000—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59446938HCID 59446938—

Reaction Conditions

Temperature0 °C

Reaction Steps

A cooled (0° C.) solution of 6-((cyclopropylmethyl)(propyl)amino)pyrimidine-4-carboxylic acid (Intermediate 21, 0.2 g; 0.85 mmol) in DCM (5 ml) was treated with triethylamine (0.13 ml; 0.93 mmol) and methyl chloroformate (0.085 ml; 1.1 mmol). After stirring at 0° C. for 30 minutes, ethyl 3-(4-aminobenzylsulfonyl)propanoate (Intermediate 42, 230 mg; 0.85 mmol) was added. After stirring at 0° C. for 5 minutes and RT for 1 hour water was added and the mixture passed through a hydrophobic frit. The solvent was removed in vacuo and the residue purified by column chromatography (silica) eluting with petroleum ether containing increasing amounts of EtOAc to give the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150519B2
Source datasetuspto-grants-2015_10
ORD IDord-d9f39a52b20947b88c7c3c560685a6d0
Source noteuspto-grants-2015_10