Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Furfuryl Alcohol | HCID 7361 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 18182475 | HCID 18182475 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 18182304 | HCID 18182304 | — |
Reaction Steps
14.1 mg of 60% oily sodium hydride was added to a mixture of 73.3 mg of 4-benzyl-5-bromo-2-chloropyrimidine (Production Example 15), 1 ml of furfuryl alcohol and 14.8 mg of cuprous iodide at room temperature, followed by stirring at 90° C. for 2 hours. Water and diethyl ether were added to the reaction solution, and the organic phase was washed with water and brine, dried over anhydrous magnesium sulfate and the solvent was removed. The residue was subjected to silica gel column chromatography using 10% ethyl acetate/hexane, to give 50.9 mg of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06599917B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-186927a5f3f640cb810079e76124280b |
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| Source note | uspto-grants-2003_07 |
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