HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851478Generated: November 2, 2026
2-Thiophenesulfonyl chloride → HCID 57476231, compound
https://huagongshe.com/reaction/1851478
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Thiophenesulfonyl chloride | HCID 85518 | — |
| Reactant | ethyl 7-amino-5-methyl-1H-indole-2-carboxylate | HCID 21218299 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 57476231 | HCID 57476231 | 91% |
Reaction Steps
To a mixed solution of ethyl 7-amino-5-methyl-1H-indole-2-carboxylate (0.60 g) and pyridine (10 mL) was added 2-thiophenesulfonyl chloride (0.66 g) under ice-cooling, and the mixture was stirred at room temperature for 15 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with ethyl acetate, washed with aqueous citric acid solution, aqueous sodium hydrogencarbonate solution and brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (ethyl acetate:hexane=3:7-5:5), and the obtained crystals were recrystallized from ethyl acetate-hexane to give the title compound (910 mg, yield 91%) as colorless needle crystals. melting point 168-169° C.
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-821e049db7bc426d8af712a7bde9ab6e |
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| Source note | uspto-grants-2015_02 |
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