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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058591Generated: October 30, 2026

Triethylamine → HCID 9889526, compound

https://huagongshe.com/reaction/1058591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantHCID 12052797HCID 12052797—
SolventDichloromethaneHCID 6344—
ProductHCID 9889526HCID 9889526—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 0.31 g (0.94 mmol) of {(1R)-1-cyclohexylmethyl-2-[4-(2-methoxyphenyl)-piperazin-1-yl]-ethyl}-amine and 0.26 mL (1.87 mmol) of triethylamine in 10 mL of dichloromethane at 0° C. was added dropwise 0.15 g (1.03 mmol) of cyclohexanecarboxylic acid chloride in 4 mL of dichloromethane. The reaction mixture was allowed to stir under nitrogen at 0° C. for one hour, and was then concentrated on a rotary evaporator, diluted with ethyl acetate and washed with saturated aqueous NaHCO3 and brine. The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated on a rotary evaporator to yield the crude product, which was purified by flash chromatography on silica gel (dichloromethane/methanol) and then converted to the dihydrochloride salt of the title compound with ethanolic HCl to yield 0.41 g (85%) as a beige solid; mp=121-131° C.; MS (+) ESI m/z=442 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518272B2
Source datasetuspto-grants-2003_02
ORD IDord-4f69fc4675604ed9ae113788661566e9
Source noteuspto-grants-2003_02