Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851625Generated: November 2, 2026

Dimethylacetamide → HCID 59136021, compound

https://huagongshe.com/reaction/1851625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylacetamideHCID 31374—
Reactant2-BromopropanedialHCID 74945—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57475964HCID 57475964—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59136021HCID 5913602129.4%

Reaction Steps

7-[(2-Ethoxyethyl) (2-thienylsulfonyl)amino]-1H-indole-2-carbothioamide (3.00 g), bromomalonaldehyde (2.32 g) and N,N-dimethylacetamide (50 mL) were stirred at 95° C. for 3 hr. The reaction mixture was diluted with ethyl acetate and water, and the ethyl acetate layer was washed successively with saturated brine and aqueous sodium bicarbonate, dried over magnesium sulfate and filtrated. The filtrate was concentrated, subjected to silica gel column chromatography and eluted with a mixture of ethyl acetate-hexane (1:1) to give a solid. The solid was dissolved in tetrahydrofuran (50 mL) and methanol (20 mL), sodium borohydride (176 mg) was added and the mixture was stirred at room temperature for 3 days. The reaction mixture was diluted with ethyl acetate and washed with 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 a mixture of ethyl acetate-hexane (2:1) to give the title compound (1.00 g, yield 29%) as an amorphous form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957070B2
Source datasetuspto-grants-2015_02
ORD IDord-ca3317fad9be4dfabe2fcec8294d2822
Source noteuspto-grants-2015_02