Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960295Generated: November 1, 2026

Lawesson's reagent → 6-chloro-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carbothioamide

https://huagongshe.com/reaction/1960295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
Reactant6-chloro-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxamideHCID 57476028—
SolventTetrahydrofuranHCID 8028—
Product6-chloro-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carbothioamideHCID 5747602991%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 6-chloro-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxamide (0.80 g), Lawesson's reagent (0.90 g) and tetrahydrofuran (15 ml) was stirred at 60° C. for 3 hr. The reaction mixture was concentrated, toluene was added, and the resulting crystals were filtrated, washed with toluene, and dried to give the title compound (0.75 g, yield 91%) as yellow crystals. melting point 228-230° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410087B2
Source datasetuspto-grants-2013_04
ORD IDord-3593b7d96c024c1cafe81f66e0cba95c
Source noteuspto-grants-2013_04