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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478360Generated: October 30, 2026

Acetic Acid → HCID 18001088, compound

https://huagongshe.com/reaction/478360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-MethylbenzaldehydeHCID 10722—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 18001077HCID 18001077—
SolventMethanolHCID 887—
ProductHCID 18001088HCID 18001088—

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of 7-chloro-5-[(4-methyl-1-piperazinyl)carbonylmethyl]-1-(2-methoxy-2-aminobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine (0.8 g) in methanol (30 ml) are added o-tolualdehyde (0.35 ml) and acetic acid (1 ml), and the mixture is stirred at 50-60° C. for 2-3 hours. To the mixture is added sodium cyanoborohydride (0.11 g) at room temperature, and the mixture is stirred for two hours. The mixture is evaporated to remove the solvent, and to the residue is added water. The mixture is extracted with ethyl acetate, and the extract is dried, and evaporated. The residue is purified by silica gel column chromatography (solvent; dichloromethane:methanol=50:1→25:1), and recrystallized from acetone/diethyl ether to give 7-chloro-5-[(4-methyl-1-piperazinyl)carbonylmethyl]-1-[2-methoxy-4-(2-methylbenzylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.71 g) as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642223B2
Source datasetuspto-grants-2003_11
ORD IDord-f6ae94a2de92412d8944c977bbcd3d0d
Source noteuspto-grants-2003_11