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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870452Generated: November 1, 2026

Acetic Acid → HCID 18001088, compound

https://huagongshe.com/reaction/1870452

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)carbonyl-methyl]-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 numberUS06096735
Source datasetuspto-grants-2000_08
ORD IDord-097102e3e66e4888bc7e1aa3f459234c
Source noteuspto-grants-2000_08