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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504743Generated: November 3, 2026

2-Thiophenesulfonyl chloride → ethyl 7-[(2-thienylsulfonyl)amino]-5-(trifluoromethoxy)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/504743

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
Reactantethyl 7-amino-5-(trifluoromethoxy)-1H-indole-2-carboxylateHCID 57476183—
SolventPyridineHCID 1049—
Productethyl 7-[(2-thienylsulfonyl)amino]-5-(trifluoromethoxy)-1H-indole-2-carboxylateHCID 5747618589.2%

Reaction Steps

To a mixture of ethyl 7-amino-5-(trifluoromethoxy)-1H-indole-2-carboxylate (2.53 g) and pyridine (50 mL) was added thiophene-2-sulfonyl chloride (1.94 g) at 0° C., and the mixture was stirred at room temperature for 4 hr, and concentrated. 1N Hydrochloric acid was added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4), and concentrated. The obtained crystals were washed with diisopropyl ether to give the title compound (3.40 g, yield 89%) as colorless crystals. The crystals were recrystallized from ethyl acetate-hexane to give colorless prism crystals. melting point 196-197° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777047B2
Source datasetuspto-grants-2010_08
ORD IDord-b986040bc8214caca0fced403f3773f7
Source noteuspto-grants-2010_08