HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422656Generated: October 29, 2026
Methyl iodide → 3-(1-(4-(1-Methyl-2-oxo-1,2-dihydropyridin-4-yl)phenyl)cyclopropyl)-6-(2-methylallyl)-6-phenyl-1,3-oxazinan-2-one
https://huagongshe.com/reaction/1422656
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(1-(4-(2-Methoxypyridin-4-yl)phenyl)cyclopropyl)-6-(2-methylallyl)-6-phenyl-1,3-oxazinan-2-one | HCID 66869568 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(1-(4-(1-Methyl-2-oxo-1,2-dihydropyridin-4-yl)phenyl)cyclopropyl)-6-(2-methylallyl)-6-phenyl-1,3-oxazinan-2-one | HCID 50905952 | 83.4% |
Reaction Steps
A mixture of 3-(1-(4-(2-methoxypyridin-4-yl)phenyl)cyclopropyl)-6-(2-methylallyl)-6-phenyl-1,3-oxazinan-2-one (26.5 mg, 0.058 mmol), K2CO3 (16 mg, 2 equiv), iodomethane (250 μL, excess) and acetonitrile (3 mL) was heated at 90° C. for 1.5 h in the microwave oven. LC-MS found the reaction was complete. The mixture was filtered, concentrated, acidified with 5% aq HCl and purified by prep HPLC to afford the title compound (22 mg, 83%). LC-MS Method 1 tR=1.68 min, m/z=455.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927539B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-c20bbec6628d4d428d4bf8947bd4277a |
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| Source note | uspto-grants-2015_01 |
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