HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960240Generated: October 25, 2026
Tetrahydrofuran → 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid
https://huagongshe.com/reaction/1960240
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylate | HCID 57475952 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylic acid | HCID 57475951 | 94.8% |
Reaction Steps
A mixture of ethyl 7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carboxylate (0.40 g), 8N aqueous sodium hydroxide solution (0.40 ml), tetrahydrofuran (5 ml) and methanol (5 ml) was stirred at 60° C. for 1 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 collected by filtration; washed with water, and dried to give the title compound (0.35 g, yield 91%) as colorless crystals. melting point >240° C. (decomposition).
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-c2cb8f42f80d4f6794db8fdb9975360c |
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| Source note | uspto-grants-2013_04 |
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