HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)- → HCID 10271284, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)- | HCID 11294484 | — |
| Reactant | HCID 22473547 | HCID 22473547 | — |
| Product | HCID 10271284 | HCID 10271284 | — |
Reaction Steps
3-(5-Bromo-2-fluorophenyl)pyridine-2-carbonitrile was coupled to 3-tributylstannyl-7-trifluoromethylimidazo[1,2-α]pyrimidine by the method of Example 32. Purification by chromatography on silica gel eluting with dichloromethane containing 4% methanol, then crystallisation from hot toluene, gave 3-[2-fluoro-5-(7-trifluoromethylimidazo[1,2-α]pyrimidin-3-yl)phenyl]pyridine-2-carbonitrile: δH (400 MHz, DMSO) 9.39 (1H, d, J 7), 8.87 (1H, dd, J 5 and 1.5), 8.33 (1H, s), 8.30 (1H, dd, J 8 and 1), 8.09 (1H, dd, J 7 and 2), 8.00-8.03 (1H, m), 7.94 (1H, dd, J 8 and 5), 7.72 (1H, dd, J 10 and 9), 7.54 (1H, d, J 7); m/z (ES+) 384.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900215B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-17f2046f85954181bab8d4d6f8b993d3 |
| Source note | uspto-grants-2005_05 |