Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746793Generated: October 31, 2026

Methyl chloroformate → HCID 59447046, compound

https://huagongshe.com/reaction/1746793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantDiisopropylamineHCID 7912—
ReactantSodium BicarbonateHCID 516892—
Reactant6-[Cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylic acidHCID 59446841—
ReactantHCID 59446860HCID 59446860—
SolventDichloromethaneHCID 6344—
ProductHCID 59447046HCID 59447046—

Reaction Conditions

Temperature0 °C

Reaction Steps

A cooled (0° C.) solution of 6-(cyclohexyl(cyclopropylmethyl)amino)pyrimidine-4-carboxylic acid (Intermediate 13, 130 mg; 0.47 mmol) in DCM was treated with diisopropylamine (90 mL; 0.52 mmol) and methyl chloroformate (40 mL; 0.52 mmol). After stirring at 0° C. for 15 minutes, ethyl 3-(4-aminobenzylsulfonyl)propanoate (Intermediate 42, 130 mg; 0.48 mmol) was added. After stirring at 0° C. for 30 minutes and RT for 1 hour, saturated sodium bicarbonate solution was added and the mixture stirred for 15 minutes. DCM was added and the layers separated. The organic extract was filtered through a hydrophobic frit and the solvent removed in vacuo. The residue was purified by column chromatography (silica) eluting with petroleum ether containing increasing amounts of EtOAc to give the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150519B2
Source datasetuspto-grants-2015_10
ORD IDord-c3c90fbe7ba2442cb13d9e0e568c7ee7
Source noteuspto-grants-2015_10