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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851626Generated: November 1, 2026

Dimethylacetamide → HCID 57475966, compound

https://huagongshe.com/reaction/1851626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylacetamideHCID 31374—
Reactant2-BromopropanedialHCID 74945—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57475962HCID 57475962—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57475966HCID 5747596617%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 7-[ethyl(2-thienylsulfonyl)amino]-1H-indole-2-carbothioamide (4.10 g), bromomalonaldehyde (3.55 g) and N,N-dimethylacetamide (30 mL) was stirred at 95° C. for 1.5 hr. To the reaction mixture was added water, and the obtained precipitate was dissolved in tetrahydrofuran (30 mL) and methanol (30 mL). After cooling in an ice bath, sodium borohydride (508 mg) was added, and the mixture was stirred at room temperature for 16 hr. The reaction mixture was concentrated and diluted with a mixture of ethyl acetate-tetrahydrofuran and washed successively with aqueous sodium bicarbonate and saturated brine. The organic layer was dried over magnesium sulfate and filtrated. The filtrate was concentrated, subjected to silica gel column chromatography, and eluted with an ethyl acetate-hexane (2:1) mixture to give the title compound (800 mg, yield 17%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-8d2d7e5f49e541e8846c8e1704901be8
Source noteuspto-grants-2015_02