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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883699Generated: October 31, 2026

Cyclohexanecarboxaldehyde → HCID 57567656, compound

https://huagongshe.com/reaction/883699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarboxaldehydeHCID 16275—
ReactantBorohydrideHCID 28123—
Reactant2-(Benzyloxy)benzaldehydeHCID 344784—
ReactantHCID 69027345HCID 69027345—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 57567656HCID 57567656—

Reaction Steps

A solution of 1-(2-aminoethyl)-N,N-diisobutyl-2-[(3,4,5-trimethoxyphenyl)amino]-1H-benzimidazole-5-carboxamide (30 mg, 1 eq) and cyclohexanecarboxaldehyde (5 mg, 0.8 eq) in methanol (0.7 ml) is stirred at a temperature of approximately 20° C. for 4 hours. Borohydride resin (48 mg, 2.5 mmol/g, Amberlite®, IRA-400) is added and the mixture is stirred for 18 hours then dichloromethane (0.5 ml) and benzyloxybenzaldehyde Wang resin (37 mg, 3.22 mmol/g, Novabiochem) are added. After stirring overnight, the mixture is filtered and the filtrate is evaporated under reduced pressure in order to produce the expected compound in the form of a beige foam (18 mg, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236965B2
Source datasetuspto-grants-2012_08
ORD IDord-51213cf7be74412eadea33b512803d40
Source noteuspto-grants-2012_08