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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358459Generated: October 31, 2026

Toluene → HCID 86099305, compound

https://huagongshe.com/reaction/2358459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantLawesson's reagentHCID 87949—
Reactant7-Chloro-1-(cyclohexylmethyl)-1H-indole-3-carboxamideHCID 68675095—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86099305HCID 8609930575%

Reaction Steps

A mixture of 7-chloro-1-(cyclohexyl)methyl-1H-indole-3-carboxylic acid amide (1.74 g, 6.0 mmol), Lawesson's reagent (4.85 g, 12.0 mmol), toluene (150 ml) and tetrahydrofuran (50 ml) was stirred at room temperature for 3 days. The reaction mixture was concentrated in vacuo and the obtained reside was purified by column chromatography eluting with 20-50% (v/v) ethyl acetate in n-heptane to afford 7-chloro-1-(cyclohexyl)methyl-1H-indole-3-carbothioic acid amide (1.38 g, 4.50 mmol). A mixture of 7-chloro-1-(cyclohexyl)methyl-1H-indole-3-carbothioic acid amide (921 mg, 3.00 mmol), 1,3-dichloroacetone (571 mg, 4.50 mmol) in toluene (30 ml) was stirred at 40° C. for 18 h. The reaction mixture was concentrated in vacuo, and the obtained crystals were washed with 10% dichloromethane (v/v) in n-heptane to give 7-chloro-3-[4-(chloromethyl)thiazol-2-yl]-1-(cyclohexyl)methyl-1H-indole (587 mg, 1.55 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763732B2
Source datasetuspto-grants-2010_07
ORD IDord-2d50d29e52934c00b8e1593ae80dcbc8
Source noteuspto-grants-2010_07