HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetophenone → t-Butyl (2-{4-[3-(4-morpholin-4-yl-phenyl)-3-oxo-propenyl]-benzoylamino}-phenyl)-carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Morpholinoacetophenone | HCID 38362 | — |
| Reactant | Tert-butyl {2-[(4-formylbenzoyl)amino]phenyl}carbamate | HCID 22668143 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | t-Butyl (2-{4-[3-(4-morpholin-4-yl-phenyl)-3-oxo-propenyl]-benzoylamino}-phenyl)-carbamate | HCID 86602775 | 90% |
Reaction Steps
To a stirred solution at room temperature of XI (210 mg, 0.62 mmol), 4′-morpholino acetophenone (227 mg, 1.11 mmol) or acetophenone derivative (1.5–2.0 equiv.) in MeOH (10 ml) was added a solution of NaOH (1.9 ml, 1N in H2O). A precipitate appeared. After 3 days, the reaction mixture was filtered off, rinsed with MeOH, air-dried and dried under vacuum to afford the title compound XXVf (295 mg, 0.56 mmol, 90% yield) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07282608B2 |
| Source dataset | uspto-grants-2007_10 |
| ORD ID | ord-b56c569ffb3244489f318879259eb87d |
| Source note | uspto-grants-2007_10 |