HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 66609624, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178505733 | HCID 178505733 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 66609624 | HCID 66609624 | 72.2% |
Reaction Steps
To 7-bromo-2-(difluoro(5-fluoropyridin-2-yl)methyl)quinazoline-4-thiol (500 mg, 1.29 mmol) in isopropanol (10 mL) were added 1N NaOH (1.94 mL, 1.94 mmol) and iodomethane (0.097 mL, 1.55 mmol) and the mixture was stirred at rt for 30 min. A brown solid formed, which was collected by filtration and washed with MeOH to afford 7-bromo-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazoline (0.373 g, 72%). 1H NMR (300 MHz, CDCl3) δ 8.45-8.51 (m, 1H), 8.26-8.32 (m, 1H), 7.93-8.03 (m, 2H), 7.74 (dd, J=1.9, 8.9 Hz, 1H), 7.54-7.65 (m, 1H), 2.61 (s, 3H); LC-MS (ESI) m/z 400/402 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633207B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-f699aec0685846a3a044a778a47c7ad9 |
| Source note | uspto-grants-2014_01 |