HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-(2-(4-(benzylcarbamoyl)phenyl)hydrazinyl)-2-(4-cyanophenyl)acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | N-benzyl-6-hydrazinylpyridine-3-carboxamide | HCID 51370238 | — |
| Reactant | Ethyl 2-(4-cyanophenyl)-3-(dimethylamino)acrylate | HCID 117601544 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 3-(2-(4-(benzylcarbamoyl)phenyl)hydrazinyl)-2-(4-cyanophenyl)acrylate | HCID 131732881 | 39% |
Reaction Steps
Combined N-benzyl-6-hydrazinylnicotinamide (126 mg, 0.520 mmol) and ethyl 2-(4-cyanophenyl)-3-(dimethylamino)acrylate (127 mg, 0.520 mmol) in ethanol (10 mL) and stirred at room temperature overnight. The reaction mixture was evaporated to give a residue which was dissolved in DCM (100 ml), extracted with saturated aqueous sodium bicarbonate (50 ml), dried with Na2SO4, and concentrated to a residue which was purified by chromatography (12 g SiO2, DCM-MeOH 0 to 10%) to give the title compound (90 mg, 39%) as an oil. MS m/z [M+H]+ 442.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040522B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-9e3097d26a8f46d082928e970a700f50 |
| Source note | uspto-grants-2015_05 |