HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 7-Bromo-2-methyl-1,6-naphthyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | (E)-4-(4-Amino-6-bromopyridin-3-yl)but-3-en-2-one | HCID 89995621 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Bromo-2-methyl-1,6-naphthyridine | HCID 89995619 | 90% |
Reaction Steps
(E)-4-(4-Amino-6-bromopyridin-3-yl)but-3-en-2-one (Preparation 66, 331 mg 1.37 mmol) and sodium thiomethoxide (97.5 mg 1.39 mmol) were stirred in ethanol (2.9 mL) at 20° C. for 50 minutes. Iodomethane (86 uL, 1.38 mmole) was added and the reaction stirred for another 45 minutes. The reaction was concentrated in vacuo and diluted with ethyl acetate (30 mL) and washed with water (10 mL). The aqueous was back extracted with ethyl acetate (5 mL) and the combined organic layers were washed with brine, dried over sodium sulfate and concentrated in vacuo to afford the title compound (275 mg, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09334286B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-77f27829e73446deb99cc615115187ac |
| Source note | uspto-grants-2016_05 |