Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Fluorobenzyl bromide | HCID 68021 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22504368 | HCID 22504368 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 9929964 | HCID 9929964 | — |
Reaction Steps
To a solution of the compound obtained in Example 11′ (3) (20,mg) in N,N-dimethylformamide (2 ml), 60% sodium hydride (4.4 mg) was added at 0° C. under nitrogen atmosphere and the mixture was stirred for 30 minutes, followed by addition of 4-fluorobenzyl bromide (2.6 mg), and the reaction mixture was stirred for further 30 minutes. The reaction solution was then poured into a saturated aqueous sodium hydrogencarbonate solution and extracted with toluene. The organic layer was washed with water and a saturated aqueous NaCl solution, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was separated using silica gel preparative thin-layer chromatography (hexane:ethyl acetate 1:1) to obtain 18 mg of the desired product as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612070B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-397e0b20a2b04a2d8ef29b0aa147be0d |
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| Source note | uspto-grants-2009_11 |
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