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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059405Generated: November 1, 2026

Ethanol → HCID 18670166, compound

https://huagongshe.com/reaction/1059405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Bromo-1-(2-pyridinyl)-1-ethanone hydrobromideHCID 2776231—
ReactantHCID 18670561HCID 18670561—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 18670166HCID 1867016656.1%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 550 mg of (10H-pyrazino[2,3-b][1,4]benzothiazin-8-yl)thioacetamide in a solvent mixture of ethanol (10 ml) with N,N-dimethylformamide (10 ml) was added 560 mg of (2-bromoacetyl)pyridine hydrobromide and the resulting mixture was heated to 60 to 70° C. for 2 hours. Then the reaction mixture was brought back to room temperature and distributed into dichloromethane and an aqueous solution of sodium bicarbonate. After extracting the organic layer, the extract was washed with water and dried over anhydrous sodium sulfate. After distilling off the solvent under reduced pressure, the crystals thus precipitated were washed successively with ethyl acetate and diethyl ether to thereby give 420 mg of the title compound as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518423B1
Source datasetuspto-grants-2003_02
ORD IDord-fff897f5e5394777a2cf409c4ef05016
Source noteuspto-grants-2003_02