Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(pyridin-2-ylmethyl)acetamide | HCID 5084090 | — |
| Reactant | 1-(Bromomethyl)-3-(tetradecyloxy)benzene | HCID 9977250 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10321644 | HCID 10321644 | — |
Reaction Steps
The title compound is prepared by the procedure of Example 27 using 2.25 g of product from Example 25, 0.881 g of product from Example 12, 0.282 g of 50% sodium hydride and 30 ml of tetrahydrofuran. The reaction is stirred at 0° C. for I hour, room temperature for 18 hours and at reflux temperature for 6 hours. The residue is purified by column chromatography (silica gel: 90% ethyl acetate/hexane) to give 1.57 g of product as pale yellow crystals. Spectral data shows the product as 2 rotomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05328921 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-820cc2fe9cbc4cee8e263f87e1b88f47 |
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| Source note | uspto-grants-1994_07 |
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