HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851445Generated: November 1, 2026
Tetrahydrofuran → 3-Methyl-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid
https://huagongshe.com/reaction/1851445
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 3-methyl-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylate | HCID 57901865 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Methyl-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid | HCID 57901712 | 94% |
Reaction Steps
A mixture of ethyl 3-methyl-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylate (1.33 g), 8N aqueous sodium hydroxide solution (2.0 mL), tetrahydrofuran (5 mL) and ethanol (10 mL) was stirred at 60° C. for 3 hr. The reaction mixture was concentrated, and water was added to the residue. The mixture was acidified with 10% aqueous citric acid solution, and the resulting crystals were filtrated, washed with water, and dried to give the title compound (1.15 g, yield 94%) as colorless crystals. melting point>263° 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-efccaf19511c463c8a5192c8725f8f2a |
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| Source note | uspto-grants-2015_02 |
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