Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Methyl 2-(4-fluorophenyl)imidazo[1,2-a]pyrazine-8-carboxylate | HCID 57438736 | — |
| Product | HCID 57438766 | HCID 57438766 | 91% |
Reaction Steps
In a sealed tube vessel was added 8M methylamine in EtOH (10 mL, 80 mmol) and 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; 2.30 g, 9.3 mmol). The mixture was heated at about 100° C. for about 1 h. The mixture was cooled to ambient temperature and the reaction mixture was partitioned between water and dichloromethane. The layers were separated. The organic layer was washed with brine, dried over Na2SO4, and filtered prior to concentrating under reduced pressure. The product was purified by silica gel chromatography using EtOAc/heptane (1:1) to give the title compound as a beige solid (2.05 g, 91%): LC/MS (Table 1, Method a) Rt=1.70 min; MS m/z: 243.3 (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-517b13d41dbc4cfd9e5e539e629e458d |
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| Source note | uspto-grants-2010_05 |
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