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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 6-chloro-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid | HCID 57476031 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-chloro-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamide | HCID 57476032 | 101.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07652133B2 |
|---|
| Source dataset | uspto-grants-2010_01 |
|---|
| ORD ID | ord-0d1d72f439eb492eb7a004dcd34fa447 |
|---|
| Source note | uspto-grants-2010_01 |
|---|