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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249082Generated: October 30, 2026

Benzaldehyde → (3S)-2-[(4-Chlorobenzylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid benzylidenehydrazide

https://huagongshe.com/reaction/1249082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantCarbon DisulfideHCID 6348—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantTriethylamineHCID 8471—
Reactant(3S)-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-3-carbohydrazideHCID 7109654—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product(3S)-2-[(4-Chlorobenzylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid benzylidenehydrazideHCID 5661420059%

Reaction Steps

(3S)-1,2,3,4-Tetrahydro-β-carboline-3-carboxylic acid hydrazide (2.44 g) is dissolved in dimethylsulfoxide (30 ml) and thereto is added benzaldehyde (2 ml). The mixture is stirred at room temperature for 2 hours and thereto are added triethylamine (1.49 ml) and carbon disulfide (0.64 ml). The mixture is stirred at room temperature for one hour and thereto is added dropwise 4-chlorobenzyl chloride (1.7 g). The mixture is stirred at room temperature for 3 hours and thereto is added water. The mixture is extracted with ethyl acetate. The extract is washed with water, dried and distilled to remove the solvent to give the title compound (3.26 g, 59%), as pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04628057
Source datasetuspto-grants-1986_12
ORD IDord-c27088c68fb9428cb9882be74605c639
Source noteuspto-grants-1986_12