Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Methyl 2-(4-fluorophenyl)imidazo[1,2-a]pyrazine-8-carboxylate | HCID 57438736 | — |
| Product | HCID 57438763 | HCID 57438763 | — |
Reaction Steps
A mixture of MeOH (18 mL) and sodium (1.1 g, 48 mmol) was stirred at ambient temperature until the sodium was consumed then 8-chloro-2-(4-fluorophenyl)-imidazo[1,2-a]pyrazine (prepared from general procedure B using 3-chloropyrazin-2-ylamine and 2-bromo-1-(4-fluorophenyl)-ethanone; 1.0 g, 4 mmol) was added. The mixture was heated at about 50° C. for about 1 h. The mixture was cooled to ambient temperature and filtered. The beige solid isolated was carried on crude. (0.98 g, 100%): LC/MS (Table 1, Method b) Rt=1.8 min; MS m/z: 244.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07709468B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-7a9de3dae3dc4da0884e74334ea093b5 |
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| Source note | uspto-grants-2010_05 |
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