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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064089Generated: October 31, 2026

Cyclohexanecarboxaldehyde → HCID 22278001, compound

https://huagongshe.com/reaction/1064089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarboxaldehydeHCID 16275—
Reactant4-(3,4-Dichloro-phenyl)-5-pyridin-4-yl-pyrazolidin-3-oneHCID 22277994—
SolventChloroformHCID 6212—
ProductHCID 22278001HCID 22278001—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 4-(3,4-Dichloro-phenyl)-5-pyridin-4-yl-pyrazolidin-3-one 0.30 g and 0.2 mL cyclohexanecarbaldehyde in chloroform 20 mL was added NaBH3(CN) 0.1 g at 0° C., the reaction was warmed 50° C. and stirred for 1 hour. The reaction was quenched with sat.NaHCO3 25 mL at 0° C. The reaction mixture was extracted with dichloromethane, 3×50 mL. The combined organic phase was washed with brine, dried over anhydrous Na2SO4. After purification by flash chromatography, the title compound was obtained as yellow solid 0.4 g. MS (ES+): 404 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967254B2
Source datasetuspto-grants-2005_11
ORD IDord-5b5724a7873a4f908b4ec667f72a705c
Source noteuspto-grants-2005_11