HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(3-Bromoimidazo[1,2-a]pyrimidin-7-yl)propan-2-ol → 2-[3-(2-Fluoro-3-(pyridin-4-yl)phenyl)imidazo[1,2-alpha]pyrimidin-7-yl]propan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(3-Bromoimidazo[1,2-a]pyrimidin-7-yl)propan-2-ol | HCID 11242282 | — |
| Reactant | [2-Fluoro-3-(pyridin-4-yl)phenyl]boronic acid | HCID 22285310 | — |
| Product | 2-[3-(2-Fluoro-3-(pyridin-4-yl)phenyl)imidazo[1,2-alpha]pyrimidin-7-yl]propan-2-ol | HCID 10132475 | — |
Reaction Steps
2-(3-Bromoimidazo[1,2-α]pyrimidin-7-yl)propan-2-ol was coupled with 2-fluoro-3-(pyridin-4-yl)benzeneboronic acid as described in Example 1 to give 2-[3-(2-fluoro-3-(pyridin-4-yl)phenyl)imidazo[1,2-α]pyrimidin-7-yl]propan-2-ol as a white solid. Bis-hydrochloride salt (from ethyl acetate/ethanol): δH (360 MHz, DMSO) 1.56 (6H, s), 7.69 (1H, dd, J 8 and 8), 7.84-7.92 (2H, m), 7.99-8.04 (1H, m), 8.21 (2H, d, J 6), 8.53 (1H, s), 8.98 (2H, d, J 6),9.30 (1H, dd, J 7 and 3); m/z (ES+) 349 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900215B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-e01cc231a7e24c519d199d1fa890020c |
| Source note | uspto-grants-2005_05 |