Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloronicotinonitrile | HCID 81079 | — |
| Reactant | 4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyl alcohol | HCID 11022807 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68886253 | HCID 68886253 | 33% |
Reaction Steps
To a mixture of [4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]phenyl]methanol (4.28 g), 2-chloro-3-cyanopyridine (2.10 g) and N,N-dimethylformamide (5.0 mL) was added sodium hydride (60%, oil, 0.66 g) under ice-cooling. The reaction mixture was stirred at 80° C. for 1 hr. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The obtained residue was subjected to silica gel column chromatography to give crystals (1.90 g, 33%) of 6-methyl-2-[4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]nicotinonitrile from a fraction eluted with ethyl acetate-hexane (1:2, v/v). Recrystallization from ethyl acetate-hexane gave pale-yellow prism crystals. melting point: 116-117° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07238716B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-447ca140c3e648a9b02f6c9a5868cbce |
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| Source note | uspto-grants-2007_07 |
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