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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058596Generated: October 29, 2026

Triethylamine → HCID 12052804, compound

https://huagongshe.com/reaction/1058596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantHCID 12052820HCID 12052820—
SolventDichloromethaneHCID 6344—
ProductHCID 12052804HCID 12052804—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 0.2 g (0.66 mmol) of {(1R)-1-cyclohexylmethyl-2-[4-(pyrimidin-2-yl)-piperazin-1-yl]-ethyl}-amine and 0.18 mL (1.32 mmol) of triethylamine in 10 mL of dichloromethane at 0° C. was added dropwise 0.11 g (0.73 mmol) of cyclohexanecarboxylic acid chloride in dichloromethane (2 mL). The reaction mixture was allowed to stir under nitrogen for one hour at 0° C. and was then concentrated on a rotary evaporator, diluted with ethyl acetate and washed with H2O 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 converted to the hydrochloride salt of the title compound with ethereal HCl to yield 0.21 g (68%) as a white solid; mp=121-123° C.; MS (+) ESI m/z=414 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518272B2
Source datasetuspto-grants-2003_02
ORD IDord-66b673b5d0204ebbba1250b7d73c070b
Source noteuspto-grants-2003_02