HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)- → 4-Fluoro-2-[6-(7-trifluoromethylimidazo[1,2-alpha]pyrimidin-3-yl)pyridin-2-yl]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)- | HCID 11294484 | — |
| Reactant | 2-(6-Bromopyridin-2-yl)-4-fluorobenzonitrile | HCID 22180778 | — |
| Product | 4-Fluoro-2-[6-(7-trifluoromethylimidazo[1,2-alpha]pyrimidin-3-yl)pyridin-2-yl]benzonitrile | HCID 10134544 | 14% |
Reaction Steps
3-Tributylstannyl-7-trifluoromethylimidazo[1,2-α]pyrimidine was coupled with 2-(6-bromopyridin-2-yl)-4-fluorobenzonitrile as in Example 1 to give 4-fluoro-2-[6-(7-trifluoromethylimidazo[1,2-α]pyrimidin-3-yl)pyridin-2-yl]benzonitrile as a pale pink solid (16 mg, 14%): δH (400 MHz, CDCl3) 7.29-7.32 (1H, m), 7.40 (1H, d, J 7), 7.53 (1H, dd, J 9 and 2), 7.66 (1H, dd, J 8 and 1), 7.88-8.03 (3H, m), 8.59 (1H, s), 10.56 (1H, d, J 7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07030128B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-e4f03d2588b74b328d0db7ece854cbd9 |
| Source note | uspto-grants-2006_04 |