HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504756Generated: October 25, 2026
2-Thiophenesulfonyl chloride → ethyl 5-(2-methoxyethoxy)-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylate
https://huagongshe.com/reaction/504756
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Thiophenesulfonyl chloride | HCID 85518 | — |
| Reactant | ethyl 7-amino-5-(2-methoxyethoxy)-1H-indole-2-carboxylate | HCID 57476192 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | ethyl 5-(2-methoxyethoxy)-7-[(2-thienylsulfonyl)amino]-1H-indole-2-carboxylate | HCID 57476193 | 53.1% |
Reaction Steps
To a mixture of ethyl 7-amino-5-(2-methoxyethoxy)-1H-indole-2-carboxylate (2.00 g) and pyridine (30 mL) was added thiophene-2-sulfonyl chloride (1.57 g) at 0° C., and the mixture was stirred at room temperature for 15 hr. The reaction mixture was concentrated, aqueous citric acid solution was added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained residue was subjected to silica gel column chromatography, and eluted with hexane-ethyl acetate (4:1-1:1, volume ratio) to give the title compound (1.62 g, yield 53%) as colorless crystals. The crystals were recrystallized from ethyl acetate-hexane to give colorless prism crystals. melting point 106-107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07777047B2 |
|---|
| Source dataset | uspto-grants-2010_08 |
|---|
| ORD ID | ord-f95f3a6061bf4806abd1bd738e7ebbbd |
|---|
| Source note | uspto-grants-2010_08 |
|---|