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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518071Generated: November 2, 2026

Water → 5-[Benzyl(1-methylethyl)amino]-3-chloropyrazine-2-carbaldehyde

https://huagongshe.com/reaction/518071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-benzyl-6-chloro-N-(1-methylethyl)pyrazin-2-amineHCID 61699183—
Product5-[Benzyl(1-methylethyl)amino]-3-chloropyrazine-2-carbaldehydeHCID 8664899970%

Reaction Steps

Phosphoryl chloride (5.6 mL) was added dropwise to DMF (12 mL) at 0° C. The mixture was stirred for 15 min, and a solution of N-benzyl-6-chloro-N-(1-methylethyl)pyrazin-2-amine (3.40 g) in DMF (3 mL) was added dropwise thereto. The mixture was stirred at 100° C. for 13 hr, water (50 mL) was added at 0° C., and the mixture was stirred at room temperature for 1 hr. The mixture was extracted with ethyl acetate. The aqueous layer was extracted again with ethyl acetate. The combined organic layer was washed with water and saturated brine, dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography (solvent gradient: 5→20% ethyl acetate/hexane) to give the title compound (2.42 g, 70%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115139B2
Source datasetuspto-grants-2015_08
ORD IDord-ecc0f572410c46278f7f49cc66eb1cfe
Source noteuspto-grants-2015_08