Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-Methylpyrimidin-4-amine | HCID 572852 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22385757 | HCID 22385757 | 41.3% |
Reaction Steps
A stirred mixture of bromoacetaldehyde diethyl acetal (3.43 ml, 22.1 mmol) in concentrated hydrobromic acid (1.1 ml) and water (1.1 ml) was heated at reflux under nitrogen for 2 h, then poured into ethanol (57 ml). The solution was neutralised to pH 7 with solid sodium hydrogen carbonate, then filtered. To the filtrate was added 4-amino-6-methylpyrimidine (1.0063 g, 9.22 mmol) and the mixture was stirred at room temperature for 30 min then at 60° C. for 19 h. After allowing to cool, the solvent was removed in vacuo and the residue was purified by flash chromatography (silica gel, 5-10% MeOH/CH2CO2) to give 0.5071 g (41%) of the title compound: 1H NMR (360 MHz, CDCl3) δ 2.54 (3H, s), 7.33 (1H, s), 7.59 (1H, s), 7.62 (1H, d, J 1.2 Hz), 8.96 (1H, s); MS (ES+) m/z 134 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06914065B2 |
|---|
| Source dataset | uspto-grants-2005_07 |
|---|
| ORD ID | ord-0a3ff447616d480d963ee31ba017ec82 |
|---|
| Source note | uspto-grants-2005_07 |
|---|