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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014682Generated: October 30, 2026

1-Butanol → HCID 57880841, compound

https://huagongshe.com/reaction/1014682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
Reactant1-Phenethylamine, (-)-HCID 75818—
Reactant2-Amino-3,5-dibromopyrazineHCID 620004—
ReactantHCID 57880841HCID 57880841—
Product(S)-1-(1-Phenylethyl)-1H-imidazo[4,5-B]pyrazin-2(3H)-oneHCID 24815089—
ProductHCID 57880841HCID 5788084143%

Reaction Steps

(S)-6-Bromo-N2-(1-phenylethyl)pyrazine-2,3-diamine. The title compound was prepared using (S)-α-methylbenzylamine (2.28 mL, 17.93 mmol), 2-amino-3,5-dibromo-pyrazine (3.00 g, 11.96 mmol), and n-BuOH (30 mL) as described in General Procedure A. The crude molecule was purified via silica gel chromatography (20-30% EtOAc in hexanes). Clean fractions were combined and condensed, and subsequently triturated from methanol with water while sonicating to afford 1.52 g (5.18 mmol, 43%) of (S)-6-bromo-N2-(1-phenylethyl)pyrazine-2,3-diamine. MS (ESI) m/z 294.0 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981893B2
Source datasetuspto-grants-2011_07
ORD IDord-178262c70cec4f65a1a8981ca6e2aece
Source noteuspto-grants-2011_07