Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzenepropanol | HCID 31234 | — |
| Reactant | HCID 18767977 | HCID 18767977 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18767869 | HCID 18767869 | — |
Reaction Steps
Sodium hydride (60% oily suspension, 111 mg, 2.79 mmol) was added to a stirred solution of 3-phenylpropanol (387mg, 2.85 mmol) in tetrahydrofuran (1 ml). After gas evolution ceased, 5-(4-fluorophenyl)-3-methyl-2-methylsulfonyl-6-(4-pyridyl)-4(3H)-pyrimidinone (100 mg, 0.279 mmol) was added and the mixture was heated at 60° C. for 30 min. The reaction mixture was partitioned between dichloromethane and water. The organic solution was washed with brine, dried and evaporated. Column chromatography on silica gel (hexane-ethyl acetate=2:1) provided the title compound. MS (m/z): 416.1 (M+H)+; C25H22FN3O2 requir. 415.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06420385B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-5b574414160b4540bd79e09219c8179b |
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| Source note | uspto-grants-2002_07 |
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