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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963259Generated: October 25, 2026

3-Cyclohexene-1-carbonyl chloride → HCID 57004125, compound

https://huagongshe.com/reaction/963259

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclohexene-1-carbonyl chlorideHCID 523058—
Reactant(R)-[1-Methyl-2-(4-thiophen-2-yl-1,2,3,6-tetrahydropyrid-1-yl)ethyl]-pyrid-2-yl-amineHCID 18660712—
SolventDichloromethaneHCID 6344—
ProductHCID 57004125HCID 5700412544.2%

Reaction Steps

A solution of the starting (R)-[1-methyl-2-(4-thiophen-2-yl-3,6-dihydro-2H-pyrid-1-yl)-ethyl]-pyrid-2-yl-amine (0.46 g, 1.5 mmol) in methylene chloride (20 ml) was cooled to 0° C., after which a solution of cyclohex-3-enecarbonyl chloride (0.222 g, 1.5 mmol) in methylene chloride (10 ml) was dropwise added under exclusion of moisture. The reaction mixture was stirred at ambient temperature overnight, then washed with 2.5N NaOH (10 ml). The separated organic layer was washed with brine (50 ml), dried over magnesium sulfate, filtered, and evaporated to dryness in vacuo. Column chromatography on 50 g of silica gel with chloroform as eluant, followed by trituration in ether with the addition of ethanolic HCl gave 0.27g of the title compound as the dihydrochloride, m.p. 92°-6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763460
Source datasetuspto-grants-1998_06
ORD IDord-e997d55740634178bf491cfc3d1247a7
Source noteuspto-grants-1998_06