HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851612Generated: November 1, 2026
Tetrahydrofuran → 6-chloro-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid
https://huagongshe.com/reaction/1851612
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 6-chloro-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylate | HCID 57476027 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-chloro-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid | HCID 57476026 | 95% |
Reaction Steps
A mixture of ethyl 6-chloro-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylate (1.00 g), 4N aqueous sodium hydroxide solution (2.3 mL), tetrahydrofuran (5 mL) and methanol (5 mL) was stirred at 50° C. for 2 hr. The reaction mixture was concentrated and acidified with 10% aqueous citric acid solution. The resulting crystals were filtrated, washed with water, and dried to give the title compound (0.88 g, yield 95%) as colorless crystals. melting point>290° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957070B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-b80aef68e3334a7d8c6648d995c3f993 |
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| Source note | uspto-grants-2015_02 |
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