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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046147Generated: October 30, 2026

Methyl chloroformate → HCID 67992236, compound

https://huagongshe.com/reaction/2046147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantDiisopropylamineHCID 7912—
ReactantAripiprazoleHCID 60795—
ReactantButyllithiumHCID 178418339—
Solvent2-MethyltetrahydrofuranHCID 7301—
ProductHCID 67992236HCID 67992236—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of diisopropylamine (0.99 mL, 7.02 mmol) in 2-methyltetrahydrofuran (33 mL) at −5° C. was added n-BuLi (2.67 mL, 2.5 M in hexanes, 6.69 mmol) slowly. After 20 minutes, the reaction was cooled to −78° C. and aripiprazole (1.50 g, 3.34 mmol) was added. After a further 10 minutes, methylchloroformate (0.65 mL, 8.36 mmol) was added. The reaction was held at −78° C. for 2 hours before allowing to warm to room temperature. After 2 hours the reaction was quenched with saturated aqueous ammonium chloride solution (30 mL) and extracted with ethyl acetate (2×30 mL). The organics were combined, washed with saturated aqueous sodium hydrogen carbonate solution (30 mL), brine (30 mL), dried over MgSO4 and concentrated. The crude product was purified by column chromatography on silica eluting with 1:1 ethyl acetate to dichloromethane to 10% methanol in 1:1 ethyl acetate to dichloromethane to give the product. The product was triturated in heptane to remove aliphatic impurities and then filtered to afford Compound-74 (0.824 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592427B2
Source datasetuspto-grants-2013_11
ORD IDord-88147804eb8e41508909dcd05edb3d84
Source noteuspto-grants-2013_11