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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646751Generated: October 28, 2026

Benzyl Alcohol → HCID 68650821, compound

https://huagongshe.com/reaction/646751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHCID 68650701HCID 68650701—
CatalystSilver(II) oxideHCID 92152—
ProductHCID 68650821HCID 6865082128%

Reaction Conditions

Temperature110 °C

Reaction Steps

Methyl 3-amino-6-(3-chloromethylphenyl)-N-methylpyrazine-2-carboxylate (18 mg, 0.06 mmol) and silver oxide (15 mg, 0.06 mmol) were added to benzyl alcohol (2 mL) and the mixture was heated to 110° C. over 15 hours. The benzyl alcohol was removed in vacuo and the residue purified by silica gel flash chromatography using ethyl acetate:hexanes (1:1) as eluent. The pure fractions were combined and concentrated then dried ill vacuo to give methyl 3-amino-6-(3-{[(phenylmethyl)oxy]methyl}phenyl)pyrazine-2-carboxylate (5.8 mg, 28% yield) as a yellow solid: MS (EI) for C20H20N3O3: 350 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704995B2
Source datasetuspto-grants-2010_04
ORD IDord-85c8658612004a018c09fed6803ebc62
Source noteuspto-grants-2010_04