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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638591Generated: October 31, 2026

Sodium Hydroxide → 3-Methyl-8-(5-methoxy-2-benzimidazolyl)thio-5,6,7,8-tetrahydroquinoline

https://huagongshe.com/reaction/1638591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloro-5-methoxy-1H-benzimidazoleHCID 519197—
ReactantThioureaHCID 2723790—
Reactant8-Bromo-3-methyl-5,6,7,8-tetrahydroquinolineHCID 13960260—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3-Methyl-8-(5-methoxy-2-benzimidazolyl)thio-5,6,7,8-tetrahydroquinolineHCID 13960262—

Reaction Steps

0.55 Gram of 2-chloro-5-methoxybenzimidazole, 0.2 g of thiourea and 10 ml of ethanol were mixed together and refluxed for 2 hours. Then, 5 ml of an aqueous solution containing 0.5 g of 3-methyl-8-bromo-5,6,7,8-tetrahydroquinoline and 0.3 g of sodium hydroxide was added thereto, and the resulting mixture was refluxed for 5 hours. After the reaction was completed, ethanol was removed by evaporation, to the residue thus obtained was added water, then extracted with chloroform, the chloroform extract was dried with anhydrous magnesium sulfate, and chloroform was removed by evaporation. The residue thus obtained was purified by means of a silica gel column chromatography (eluent: dichloromethane/methanol=100/1) to yield 0.5 g of 8-(5-methoxy-2-benzimidazolyl)thio-3-methyl-5,6,7,8-tetrahydroquinoline in the form of colorless caramel-like substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880815
Source datasetuspto-grants-1989_11
ORD IDord-3faac28f976a428db17bd2f030016673
Source noteuspto-grants-1989_11