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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946815Generated: November 3, 2026

Methyl chloroformate → HCID 59447046, compound

https://huagongshe.com/reaction/1946815

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 numberUS08399448B2
Source datasetuspto-grants-2013_03
ORD IDord-2601874a463c40b4a147f8c361d6941e
Source noteuspto-grants-2013_03