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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711344Generated: October 30, 2026

Methyl chloroformate → HCID 118491993, compound

https://huagongshe.com/reaction/711344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 118492065HCID 118492065—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118491993HCID 118491993112.1%

Reaction Steps

To a solution of (1S,8aS)-N-((R)-1-(3-chloro-5-(trifluoromethyl)phenyl)ethyl)-N-methyl-6-oxo-1-o-tolylhexahydropyrrolo[1,2-a]pyrazine-2(1H)-carboxamide (300 mg, 0.61 mmol) in anhydrous THF (20 mL) under N2 atmosphere was added LiHMDS (2.3 mL, 1 M in THF, 2.3 mmol) at −60° C. The reaction was stirred for 30 min followed by addition of methyl carbonochloridate (134 mg, 1.43 mmol). After stirring for another 3 h at room temperature, the reaction was quenched with water at 0° C. and then extracted with EtOAc (2×30 mL). The combined organic layers were dried over anhydrous Na2SO4 and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH=20/1 to 10/1) to give the title compound (220 mg, yield: 59%); m/z (ES+): 610 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181259B2
Source datasetuspto-grants-2015_11
ORD IDord-02920aa3b1ed4cd0a4298dad7ed171ec
Source noteuspto-grants-2015_11