HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-4,6-dichloropyrimidine → HCID 51353725, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-4,6-dichloropyrimidine | HCID 65522 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1227911-03-6 | HCID 51357959 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 51353725 | HCID 51353725 | 94.1% |
Reaction Conditions
| Temperature | 160 °C |
|---|
Reaction Steps
In a 2-5 mL microwave vessel Hunig's base (0.59 mL, 3.35 mmol) was added to [(2S,5R)-5-methyl-2-morpholinyl]methanol hydrochloride (208 mg, 1.12 mmol) in CH3CN (3 mL), and then 2-amino-4,6-dichloropyrimidine (174 mg, 1.06 mmol) was added. The mixture was heated with stirring in a microwave reactor at 160° C. for 1 hour. HPLC indicated complete conversion. The mixture was filtered through a 0.45 um filter disc, evaporated, and the product was purified further by chomatography (Analogix SF25-40 g silica column) eluting with 2-5% CH3OH—CHCl3 to afford the title compound (258 mg) as a white foam. LC-MS (ES) m/z=260 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08697685B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-150e27b893b84c379f5dbb4ec15b9ceb |
| Source note | uspto-grants-2014_04 |