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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188673Generated: October 29, 2026

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

https://huagongshe.com/reaction/2188673

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 numberUS08324201B2
Source datasetuspto-grants-2012_12
ORD IDord-7ee05bc0c1cf4af298525e3ed6272370
Source noteuspto-grants-2012_12