Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(pyridin-2-ylmethyl)acetamide | HCID 5084090 | — |
| Reactant | HCID 10045489 | HCID 10045489 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10004024 | HCID 10004024 | 33.7% |
Reaction Steps
The title compound is prepared by the procedure of Example 27 using 2.45 g of product from Example 22, 0.960 g of product from Example 12, 0.322 g of washed 50% sodium hydride and 30 ml of tetrahydrofuran. The reaction is stirred at 0° C. for 1 hour, room temperature for 18 hours; followed by heating at reflux temperature for 6 hours. The residue is purified by column chromatography (silica gel: 80% ethyl acetate/hexane) to give 0.976 g of the desired product as a yellow oil. The spectral data shows the presence of 2 rotomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05208247 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-d09ecf70b30b4f1d882d81c75e4cfcf2 |
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| Source note | uspto-grants-1993_05 |
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