HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960241Generated: October 26, 2026
Ammonia → 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamide
https://huagongshe.com/reaction/1960241
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid | HCID 57475951 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxamide | HCID 57475953 | 67% |
Reaction Steps
To a mixture of 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid (17.20 g), 1H-1,2,3-benzotriazol-1-ol (8.29 g) and N,N-dimethylformamide (150 ml) was added N-[3-(dimethylamino)propyl]-N,N-ethylcarbodiimide hydrochloride (11.8 g) at room temperature, and the mixture was stirred at 50° C. for 20 min. The mixture was allowed to cool to room temperature, and 28% aqueous ammonia (3.4 ml) was added. The reaction mixture was stirred at room temperature for 2 hr, and water was added. The mixture was acidified with 10% aqueous citric acid solution, and the resulting crystals were filtrated, washed with water, washed with cooled ethyl acetate, and dried to give the title compound (11.47 g, yield 67%) as colorless crystals. melting point 244-245° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410087B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-1a6d001f2b70456a9e78e333a2f3e28b |
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| Source note | uspto-grants-2013_04 |
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