HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetylpyrazine → N-(2-Aminophenyl)-4-((4-(2-methylimidazo[1,2-a]pyridin-3-yl)pyrimidin-2-ylamino)methyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetylpyrazine | HCID 30914 | — |
| Reactant | 1-{2-Methylimidazo[1,2-a]pyridin-3-yl}ethan-1-one | HCID 2735255 | — |
| Reactant | N-(2-aminophenyl)-4-((4-(pyrazin-2-yl)pyrimidin-2-ylamino)methyl)benzamide | HCID 44570891 | — |
| Product | N-(2-Aminophenyl)-4-((4-(2-methylimidazo[1,2-a]pyridin-3-yl)pyrimidin-2-ylamino)methyl)benzamide | HCID 58930542 | — |
Reaction Steps
Title compound was obtained according to the scheme 6 similarly to the compound 26a (Example 29) using instead of 1-pyrazin-2-yl-ethanone as the starting material the ketone 333 (Table 11). Characterization of the title compound is provided in the Table 12.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07253204B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-784bdba57de24c94ade49cbe0dc3d4bc |
| Source note | uspto-grants-2007_08 |