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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023221Generated: November 1, 2026

Methyl chloroformate → HCID 178502261, compound

https://huagongshe.com/reaction/1023221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantTriethylamineHCID 8471—
ReactantHCID 178478587HCID 178478587—
SolventDichloromethaneHCID 6344—
ProductHCID 178502261HCID 17850226130,809.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

The title compound was prepared from Trans-4-[2-(4-Benzo[1,3]dioxol-4-yl-piperazin-1-yl)-ethyl]-cyclohexylamine hydrochloride (Intermediate A) (25 mg, 0.068 mmol) and triethylamine (20.6 mg, 28.4 μl, 204 μmol) in dichloromethane (1 mL). Methyl carbonochloridate (7.06 mg, 5.78 μl, 0.075 μmol) was added to the mixture stirring at 0° C. The ice bath was removed and the reaction mixture was stirred for 1 hour at room temp. The reaction was diluted with dichloromethane and quenched with sat NaHCO3 (4 mL). The aqueous layer was extracted with DCM (1×5 mL). The organic layers were dried over MgSO4 and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 10 g, 0% to 15% MeOH in dichloromethane) to yield the title compound as a white solid (9 mg, 34%), MS (ISP) m/z=390.3 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722683B2
Source datasetuspto-grants-2014_05
ORD IDord-ca48f750bf954b248fb021f97574800c
Source noteuspto-grants-2014_05