HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibutyltin oxide → HCID 10292839, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibutyltin oxide | HCID 61221 | — |
| Reactant | HCID 57438128 | HCID 57438128 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10292839 | HCID 10292839 | — |
Reaction Steps
A suspension of 4-{2-fluoro-5-[3-(1-hydroxy-1-methylethyl)-imidazo[1,2-b][1,2,4]triazin-7-yl]phenyl}pyrimidine-5-carboxylic acid amide (50 mg, 0.13 mmol) was formed in dry toluene (50 ml). Dibutyltin oxide (6 mg, 0.03 mmol) was added and the mixture heated at reflux for 18 h. The solvent was removed under reduced pressure then purification by chromatography (silica gel, 3% MeOH/CH2Cl2) gave the title compound as a yellow solid: 1H NMR (400 MHz, CDCl3) δ 1.72 (6H, s), 3.23 (1H, s), 7.45 (1H, dd, J 9, 1 Hz), 8.24-8.29 (1H, m), 8.30 (1H, s), 8.42 (1H, dd, J 7, 2 Hz), 8.81 (1H, s), 9.14 (1H, s), 9.51 (1H, s); MS (ES+) m/z 376 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06936608B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-249dd1e319a84df8bb9dd8614f586410 |
| Source note | uspto-grants-2005_08 |