HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromo-7-(trifluoromethyl)imidazo[1,2-a]pyrimidine → HCID 10177917, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromo-7-(trifluoromethyl)imidazo[1,2-a]pyrimidine | HCID 11391462 | — |
| Reactant | HCID 22285298 | HCID 22285298 | — |
| Product | HCID 10177917 | HCID 10177917 | — |
Reaction Steps
3-Bromo-7-trifluoromethylimidazo[1,2-α]pyrimidine was coupled with 5′-(5,5-dimethyl-[1,3,2]dioxaborinan-2-yl)-2′-fluorobiphenyl-3-carbonitrile as described in Example 65 to give 2′-fluoro-5′-(7-trifluoromethylimidazo[1,2-α]pyrimidin-3-yl)biphenyl-3-carbonitrile as a yellow solid: δH (360 MHz, CDCl3) 7.28 (1H, d, J 7), 7.40-7.46 (1H, m), 7.55-7.64 (3H, m), 7.72-7.75 (1H, m), 7.83 (1H, dd, J 7 and 1), 7.89 (1H, d, J 1), 8.11 (1H, s), 8.75 (1H, d, J 7); m/z (ES+) 383 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900215B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-363b1ca27c2248cb8ef85427e31e1d59 |
| Source note | uspto-grants-2005_05 |