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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844537Generated: October 29, 2026

Water → 5-[2-(Methylthio)ethoxy]pyrazin-2-amine

https://huagongshe.com/reaction/1844537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroformHCID 6212—
ReactantSodium hydrideHCID 24758—
Reactant2-Amino-5-bromopyrazineHCID 599539—
Reactant1-(Methylthio)ethanolHCID 18425401—
CatalystCopperHCID 23978—
SolventAcetoneHCID 180—
SolventAmmoniaHCID 222—
SolventMethanolHCID 887—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product5-[2-(Methylthio)ethoxy]pyrazin-2-amineHCID 58328437—

Reaction Steps

According to the method described in WO2007007886, sodium hydride (50% oily product) (314 mg) was added to methylthioethanol (7.88 mL) under cooling with ice and stirring, and then copper (490 mg) and 2-amino-5-bromopyrazine (1.00 g) were added thereto. The reaction mixture was placed in an autoclave and heated and stirred at 160° C. for about 5 hours. After cooling, the reaction mixture was diluted with water (50 mL) and ethyl acetate (50 mL), and 25% aqueous ammonia (2 mL) was added to the mixture to make it basic. The reaction mixture was filtrated through Celite, and the organic layer and the aqueous layer were separated. The aqueous layer was extracted with ethyl acetate (50 mL×2), and the extracts and the organic layer were combined, dried over anhydrous sodium sulfate, and filtrated. The solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate=1:1) and then by preparative TLC (chloroform:methanol=10:1, then NH silica gel, hexane:acetone=3:1) to give the title compound as white powder crystals (59.2 mg, yield: 6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946440B2
Source datasetuspto-grants-2015_02
ORD IDord-4cc1a492ac6340fea871073c18c92d13
Source noteuspto-grants-2015_02