Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66990569 | HCID 66990569 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66990889 | HCID 66990889 | — |
Reaction Steps
Potassium carbonate (0.065 g) and morpholine (0.041 mL) were added to an acetone (3.0 mL) solution of tert-butyl 2-(2-(benzyloxy)-4-(2-bromoethoxy)benzamido)-4-phenylbenzoate (0.094 g), followed by heating to reflux for 45 minutes. The reaction mixture was cooled to room temperature, and potassium carbonate (0.022 g) and morpholine (0.014 mL) were added thereto, followed by heating to reflux for 2 hours and 30 minutes. The reaction mixture was cooled to room temperature, and then water, a saturated aqueous solution of sodium bicarbonate, and ethyl acetate were added thereto. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 100-91% chloroform/methanol] to obtain 0.059 g of tert-butyl 2-(2-(benzyloxy)-4-(2-(morpholin-4-yl)ethoxy)benzamido)-4-phenylbenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492582B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-10dbe970c2da40d0a569fcb42e85bea7 |
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| Source note | uspto-grants-2013_07 |
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