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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842630Generated: October 30, 2026

Triethylamine → HCID 12052798, compound

https://huagongshe.com/reaction/842630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Methylcyclohexanecarbonyl chlorideHCID 4189245—
ReactantHCID 10904095HCID 10904095—
SolventDichloromethaneHCID 6344—
ProductHCID 12052798HCID 12052798100.3%

Reaction Steps

To a solution of 0.30 g (0.87 mmol) of {(1R)-1-cyclohexylmethyl-2-[4-(2-methoxyphenyl)-piperazin-1-yl]-ethyl}-methyl-amine and 0.25 mL (1.74 mmol) of triethylamine in 10 mL of dichloromethane at 0° C. was added dropwise 0.21 g (1.31 mmol) of 1-methyl-cyclohexanecarboxylic acid chloride in 4 mL of dichloromethane. The reaction mixture was allowed to stir under nitrogen overnight at ambient temperature, and was then concentrated on a rotary evaporator, diluted with ethyl acetate and washed with 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 (86%) of white solid; mp=208-210° C.; MS(+)ESI m/z=470 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376494B1
Source datasetuspto-grants-2002_04
ORD IDord-4c298f547c1a4b968d6ade688137d9af
Source noteuspto-grants-2002_04