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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180812Generated: October 26, 2026

Acetophenone → t-Butyl (2-{4-[3-(4-morpholin-4-yl-phenyl)-3-oxo-propenyl]-benzoylamino}-phenyl)-carbamate

https://huagongshe.com/reaction/1180812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetophenoneHCID 7410—
ReactantSodium HydroxideHCID 14798—
Reactant4-MorpholinoacetophenoneHCID 38362—
ReactantTert-butyl {2-[(4-formylbenzoyl)amino]phenyl}carbamateHCID 22668143—
SolventMethanolHCID 887—
Productt-Butyl (2-{4-[3-(4-morpholin-4-yl-phenyl)-3-oxo-propenyl]-benzoylamino}-phenyl)-carbamateHCID 8660277590%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282608B2
Source datasetuspto-grants-2007_10
ORD IDord-b56c569ffb3244489f318879259eb87d
Source noteuspto-grants-2007_10