HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromo-7-(trifluoromethyl)imidazo[1,2-a]pyrimidine → 3-[2-Fluoro-3-(pyridin-4-yl)phenyl]-7-trifluoromethylimidazo[1,2-alpha]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromo-7-(trifluoromethyl)imidazo[1,2-a]pyrimidine | HCID 11391462 | — |
| Reactant | [2-Fluoro-3-(pyridin-4-yl)phenyl]boronic acid | HCID 22285310 | — |
| Product | 3-[2-Fluoro-3-(pyridin-4-yl)phenyl]-7-trifluoromethylimidazo[1,2-alpha]pyrimidine | HCID 10269751 | — |
Reaction Steps
3-Bromo-7-trifluoromethylimidazo[1,2-α]pyrimidine was coupled with 2-fluoro-3-(pyridin-4-yl)benzeneboronic acid as described in Example 1 to give 3-[2-fluoro-3-(pyridin-4-yl)phenyl]-7-trifluoromethylimidazo[1,2-α]pyrimidine as a white solid. Bis-hydrochloride salt (from ethyl acetate/ethanol): δH (400 MHz, DMSO) 7.64-7.70 (2H, m), 7.95-8.01 (2H, m), 8.37 (1H, s), 8.39 (2H, s), 9.05-9.07 (2H, m), 9.40 (1H, dd, J 7 and 3); m/z (ES+) 359 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900215B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-492af667be1d4091bb46283465872191 |
| Source note | uspto-grants-2005_05 |