HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 4-[[4-fluoro-3-[4-(3-methylpyridin-2-yl)oxypiperidine-1-carbonyl]phenyl]methyl]-2H-phthalazin-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Fluoro-3-methylpyridine | HCID 242722 | — |
| Reactant | 4-(4-fluoro-3-(4-hydroxypiperidine-1-carbonyl)benzyl)phthalazin-1(2H)-one | HCID 44199316 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 4-[[4-fluoro-3-[4-(3-methylpyridin-2-yl)oxypiperidine-1-carbonyl]phenyl]methyl]-2H-phthalazin-1-one | HCID 57791816 | — |
Reaction Steps
A solution of crude 4-[[4-fluoro-3-(4-hydroxypiperidine-1-carbonyl)phenyl]methyl]-2H-phthalazin-1-one (2a) (50 mg, 0.131 mmol) in N,N-dimethylacetamide (1 mL) was treated with sodium hydride (60% in mineral oil; 3.8 mg, 0.157 mmol) and the reaction was left stirring at ambient temperature until effervescence had stopped. 2-fluoro-3-methylpyridine (16 mg, 0.144 mmol) was then added and the reaction mixture sealed into a microwave tube, heated to 170° C. and held at that temperature for 250 seconds before cooling to ambient temperature. The mixture was then purified by preparative HPLC to afford the desired material; m/z (LC-MS, ESI+), RT=4.22 (M+H 473.2)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129380B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-708e77a8e02f45a3a6e3f06438dc8fb6 |
| Source note | uspto-grants-2012_03 |