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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994729Generated: October 29, 2026

Ammonia → 6-chloro-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamide

https://huagongshe.com/reaction/1994729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantCitric AcidHCID 311—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant6-chloro-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acidHCID 57476031—
SolventDimethylformamideHCID 6228—
Product6-chloro-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamideHCID 57476032101.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 6-chloro-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid (0.69 g), 1H-1,2,3-benzotriazol-1-ol (0.31 g) and N,N-dimethylformamide (10 ml) was added N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (0.44 g) at room temperature, and the mixture was stirred at 50° C. for 20 min, and allowed to cool to room temperature. 28% Aqueous ammonia (0.30 ml) was added, and the reaction mixture was stirred at room temperature for 2 hr, and acidified with 10% aqueous citric acid solution. The resulting crystals were filtrated, washed with water, and dried to give the title compound (0.70 g, quantitative) as colorless crystals. melting point 225-226° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652133B2
Source datasetuspto-grants-2010_01
ORD IDord-0d1d72f439eb492eb7a004dcd34fa447
Source noteuspto-grants-2010_01