HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → HCID 57880841, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | 1-Phenethylamine, (-)- | HCID 75818 | — |
| Reactant | 2-Amino-3,5-dibromopyrazine | HCID 620004 | — |
| Reactant | HCID 57880841 | HCID 57880841 | — |
| Product | (S)-1-(1-Phenylethyl)-1H-imidazo[4,5-B]pyrazin-2(3H)-one | HCID 24815089 | — |
| Product | HCID 57880841 | HCID 57880841 | 43% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981893B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-178262c70cec4f65a1a8981ca6e2aece |
| Source note | uspto-grants-2011_07 |