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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669371Generated: October 26, 2026

3-[(2-Methoxyethoxy)carbonylamino]benzaldehyde → 4-hydroxy-3-[3-[3-[(2-methoxyethoxy)carbonylamino]phenyl]-1-oxo-2-propenyl]-1,6-dimethyl-2(1H)-pyridinone

https://huagongshe.com/reaction/1669371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[(2-Methoxyethoxy)carbonylamino]benzaldehydeHCID 23131806—
Reactant2(1H)-Pyridone, 3-acetyl-4-hydroxy-1,6-dimethyl-HCID 54691703—
SolventEthanolHCID 702—
Product4-hydroxy-3-[3-[3-[(2-methoxyethoxy)carbonylamino]phenyl]-1-oxo-2-propenyl]-1,6-dimethyl-2(1H)-pyridinoneHCID 13634424860.7%

Reaction Steps

According to the same manner as that of Example a-1 except that 1.00 g of 3-[(2-methoxyethoxy)carbonylamino]benzaldehyde was used in place of 3-[(methoxycarbonyl)methoxy]benzaldehyde, 0.742 g of 3-acetyl-4-hydroxy-1,6-dimethyl-2(1H)-pyridinone was used in place of 3-acetyl-4-hydroxy-6-methyl-2(1H)-pyridinone, and 20 ml of ethanol was used in place of pyridine, 0.96 g of 4-hydroxy-3-[3-[3-[(2-methoxyethoxy)carbonylamino]phenyl]-1-oxo-2-propenyl]-1,6-dimethyl-2(1H)-pyridinone [Compound No. (42a)] was obtained as a yellow crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989478B2
Source datasetuspto-grants-2011_08
ORD IDord-46fa6e5c6e8948a3b372101c7cbf1405
Source noteuspto-grants-2011_08