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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698242Generated: November 2, 2026

Benzyl chloroformate → HCID 66727525, compound

https://huagongshe.com/reaction/1698242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 59278510HCID 59278510—
SolventDichloromethaneHCID 6344—
ProductHCID 66727525HCID 66727525—

Reaction Steps

To a chilled (0° C.) solution of [(S)-1-(2-carbamoyl-piperidin-4-yl)-propyl]-carbamic acid tert-butyl ester (780 mg, 2.73 mmol) in methylene chloride (25 mL) was added DIPEA (0.41 mL, 2.9 mmol) followed by benzylchloroformate (723 μL, 4.1 mmol). After 1 hour, the reaction was diluted with dichloromethane (200 mL), washed with saturated ammonium chloride, brine, dried over sodium sulfate, filtered and concentrated to afford 4-((S)-1-tert-butoxycarbonylamino-propyl)-2-carbamoyl-piperidine-1-carboxylic acid benzyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163918B2
Source datasetuspto-grants-2012_04
ORD IDord-0f4d283847184e2ba874393f67980477
Source noteuspto-grants-2012_04