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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789020Generated: October 30, 2026

(3-Oxetanyl) 2-(2,3-dichlorophenylmethylene)-3-oxobutanoate → 3-Methyl 5-(3-oxetanyl) 4-(2,3-dichlorophenyl)-2-(fluoromethyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate

https://huagongshe.com/reaction/1789020

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Oxetanyl) 2-(2,3-dichlorophenylmethylene)-3-oxobutanoateHCID 57031759—
ReactantMethyl 3-amino-4-fluoro-2-butenoateHCID 73668923—
Solventtert-ButanolHCID 6386—
Product3-Methyl 5-(3-oxetanyl) 4-(2,3-dichlorophenyl)-2-(fluoromethyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylateHCID 70087688—

Reaction Steps

A solution of the product of step (a) (2.9 g, 7.6 mmoles) and methyl 3-amino-4-fluoro-2-butenoate (1 g, 7.6 mmoles) in dry tert-butanol (20 ml) was heated to 60° (oil bath temperature) for 16 hours. The solution was allowed to cool to room temperature and the solvent removed in vacuo. Chromatography on silica, eluting with dichloromethane/ethyl acetate mixtures afforded the title compound as an oil which crystallised on addition of petroleum ether (60°-80° ). The solid was recrystallised from petroleum ether (60°-80° )/acetone to afford the title compound 1.03 g, mp 155°-6°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04686217
Source datasetuspto-grants-1987_08
ORD IDord-3c7b27071d2a4a3aac8df5aa0a19735f
Source noteuspto-grants-1987_08