HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-[4-[5-Methyl-2-(2-naphthyl)-4-oxazolylmethoxy]benzyloxy]nicotinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloronicotinonitrile | HCID 81079 | — |
| Reactant | 4-[5-Methyl-2-(2-naphthyl)-4-oxazolylmethoxy]benzyl alcohol | HCID 68883359 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[4-[5-Methyl-2-(2-naphthyl)-4-oxazolylmethoxy]benzyloxy]nicotinonitrile | HCID 68887101 | 78% |
Reaction Steps
To a mixture of 4-[5-methyl-2-(2-naphthyl)-4-oxazolylmethoxy]benzyl alcohol (4.00 g), 2-chloro-3-cyanopyridine (2.41 g) and N,N-dimethylformamide (80 mL) was gradually added sodium hydride (60%, oil, 700 mg) under ice-cooling. After stirring the reaction mixture at room temperature for 2 hrs, water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over anhydrous magnesium sulfate and concentrated. Recrystallization from ethyl acetate-isopropyl ether gave colorless prism crystals (4.02 g, 78%) of 2-[4-[5-methyl-2-(2-naphthyl)-4-oxazolylmethoxy]benzyloxy]nicotinonitrile. melting point: 145-146° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238716B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-1626ba7f2b6044958bddee4710476e0f |
| Source note | uspto-grants-2007_07 |