Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 18542676 | HCID 18542676 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18542746 | HCID 18542746 | — |
Reaction Steps
To a solution of 3-[3-[N-[4-(1-t-butoxycarbonylpiperidin-4-yloxy)phenyl]amino]-1-(E)-propenyl]benzonitrile (1.00 g) in N,N-dimethylformamide (20 ml) were added potassium carbonate (0.96 g) and ethyl bromoacetate (0.62 ml). The mixture was stirred at 70° C. for 9 hours. After addition of water, the reaction mixture was extracted with ethyl acetate. The extract was washed with brine. The organic layer was dried over anhydrous magnesium sulfate, filtered and the filtrate concentrated in vacuo. The residue was purified by chromatography on a silica gel column using hexane/ethyl acetate=2/1 as an eluant to give the desired compound (1.31 g, yield quantitative) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06555556B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-9cd60a6f63a042f596046432d10f5279 |
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| Source note | uspto-grants-2003_04 |
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