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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984441Generated: October 29, 2026

Cyclohexanecarboxaldehyde → HCID 22558437, compound

https://huagongshe.com/reaction/984441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarboxaldehydeHCID 16275—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantAcetic acid methylene chlorideHCID 21922555—
ReactantHCID 22558368HCID 22558368—
SolventDichloromethaneHCID 6344—
ProductHCID 22558437HCID 22558437—

Reaction Steps

A stirred solution of 48 mg of N-[3-methoxy-4-(5-oxazolyl)phenyl]-N′-[1,1-dimethyl-2-(1-piperazinyl)ethyl]oxalamide (1.2 mmol) and 13 mg of cyclohexanecarboxaldehyde (1.2 mmol) in 1 ml of a 5% acetic acid/dichloromethane mixture was treated with a solution of 38 mg of sodium triacetoxyborohydride (1.8 mmol) in 1 ml of a 5% acetic acid/dichloromethane mixture. After stirring overnight at room temperature the reaction mixture was diluted with 10 ml of dichloromethane and washed with 8 ml of a sodium bicarbonate solution followed by 8 ml of water. The organic layer was then evaporated and purified using flash chromatography on a silica gel column eluting with 5% methanol/dichloromethane to give after evaporation of the fractions 14.3 mg (0.3 mmol, 25%) of N-[2-[4-(cyclohexylmethyl)-1-piperazinyl-1,1-dimethylethyl]-N′-[3-methoxy-4-(5-oxazolyl)phenyl]oxalamide in the form of a white solid. MS: m/e 498.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867299B2
Source datasetuspto-grants-2005_03
ORD IDord-58b5b70373ff484fa17127d5319457a0
Source noteuspto-grants-2005_03