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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851571Generated: November 3, 2026

Dimethylacetamide → N-methyl-N-[4-methyl-2-(1,3-thiazol-2-yl)-1H-indol-7-yl]thiophene-2-sulfonamide

https://huagongshe.com/reaction/1851571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylacetamideHCID 31374—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
Reactant4-methyl-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carbothioamideHCID 57476008—
SolventEthyl AcetateHCID 8857—
ProductN-methyl-N-[4-methyl-2-(1,3-thiazol-2-yl)-1H-indol-7-yl]thiophene-2-sulfonamideHCID 5790159143%

Reaction Steps

A mixed solution of 4-methyl-7-[methyl(2-thienylsulfonyl)amino]-1H-indole-2-carbothioamide (0.20 g), 1-bromo-2,2-diethoxyethane (0.23 mL) and N,N-dimethylacetamide (10 ml) was stirred at 100° C. for 6 hr. The reaction solution was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (ethyl acetate:hexane=25:75-35:65), and the obtained oil was crystallized from ethyl acetate-hexane to give the title compound (92 mg, yield 43%) as pale-yellow prism crystals. melting point 159-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-1fc8b3471dd7433093729c97be2a73e6
Source noteuspto-grants-2015_02