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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478281Generated: October 30, 2026

3-Bromo-4-fluorobenzaldehyde → Methyl 7-benzyl-4-(3-bromo-4-fluorophenyl)-2-methyl-5-oxo-1,4,5,6,7,8-hexahydro[1,7]naphthyridine-3-carboxylate

https://huagongshe.com/reaction/478281

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-fluorobenzaldehydeHCID 173604—
ReactantMethyl 3-aminocrotonateHCID 643918—
Reactant1-Benzylpiperidine-3,5-dioneHCID 11138174—
SolventEthanolHCID 702—
ProductMethyl 7-benzyl-4-(3-bromo-4-fluorophenyl)-2-methyl-5-oxo-1,4,5,6,7,8-hexahydro[1,7]naphthyridine-3-carboxylateHCID 1139757953.6%

Reaction Steps

A solution of methyl 3-aminocrotonate (0.58 g, 5 mmol), 3-bromo-4-fluorobenzaldehyde (1.0 g, 5 mmol) and N-benzylpiperidine-3,5-dione (Ziegler, J. Amer. Chem. Soc. (1973), 95, 7458-7464) (1.1 g, 5 mmol) in ethanol (5 mL) was heated at reflux in a sealed tube for 24 hours and concentrated. Purification of the residue on silica gel eluting with 5% ethanol/methylene chloride provided the title compound (1.3 g) as a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642222B2
Source datasetuspto-grants-2003_11
ORD IDord-c188213bef0140bb940aca3d4b7ef567
Source noteuspto-grants-2003_11