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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994710Generated: October 30, 2026

Lawesson's reagent → 4-methyl-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carbothioamide

https://huagongshe.com/reaction/1994710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
Reactant4-methyl-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamideHCID 57476006—
SolventTetrahydrofuranHCID 8028—
Product4-methyl-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carbothioamideHCID 5747600884%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-methyl-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamide (1.78 g), Lawesson's reagent (2.26 g) and tetrahydrofuran (120 ml) was stirred at 60° C. for 2 hr. The reaction solution was concentrated under reduced pressure, and the obtained oil was crystallized from dichloromethane-toluene to give the title compound (1.56 g, yield 84%) as pale-yellow crystals. MS: 366 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652133B2
Source datasetuspto-grants-2010_01
ORD IDord-553330c360c341e384440b4fe190e48b
Source noteuspto-grants-2010_01