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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333628Generated: October 26, 2026

Water → HCID 67432957, compound

https://huagongshe.com/reaction/333628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Amino-3-benzyl-5-(4-methoxyphenyl)pyrazineHCID 11300786—
ReactantHCID 14946077HCID 14946077—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductHCID 67432957HCID 67432957—

Reaction Conditions

Temperature55 °C

Reaction Steps

Under an argon atmosphere, to a solution of 3-benzyl-5-(4-methoxyphenyl)pyrazin-2-amine (12) (synthesized by the process of M. Adamczyk, et al., Org. Prep. Proced. Int., 33, 477-485 (2001)) (500 mg, 1.72 mmol) in pyridine (8 mL) were successively added 4-(dimethylamino)pyridine (21.0 mg, 172 μmol) and 2-(4-methoxyphenyl)propanoyl chloride (16) prepared above at room temperature, and the mixture was heated with stirring at 55° C. for 14 hours. After cooling to room temperature, to the mixture was added water and the product was extracted with dichloromethane (×3). The combined organic extract was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residual pyridine was azeotropically removed with toluene (×3). The residue was purified twice by column chromatography (silica gel 50 g, dichloromethane/ethyl acetate=9/1, and silica gel 50 g, n-hexane/ethyl acetate=9/1→6/1) to give Compound 11w (942 mg, <quant.) as a colorless foamy solid containing some impurities.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883432B2
Source datasetuspto-grants-2014_11
ORD IDord-c8b0c487bf334e168c20dfb08548ff1d
Source noteuspto-grants-2014_11