Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199985Generated: October 31, 2026

2-Chlorobenzaldehyde → HCID 131716322, compound

https://huagongshe.com/reaction/1199985

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
Reactant3-Oxo-3-phenyl-N-(pyridin-2-yl)propanimidic acidHCID 268038—
ReactantHCID 70357192HCID 70357192—
SolventEthanolHCID 702—
ProductHCID 131716322HCID 131716322—

Reaction Steps

A solution of N-(pyrid-2-yl)-3-phenyl-3-oxopropionamide (0.84 g, 3.5 mM--see Preparation 15), 2-chlorobenzaldehyde (0.49 g, 3.5 mM) and 4-(2-methylimidazo[4,5-c]pyrid-1-yl)butyl 3-aminobut-2-enoate (1.01 g, 3.5 mM--see Preparation 13) in absolute ethanol (20 cm3) was heated at reflux, under nitrogen, for 16 hours. The cooled solution was evaporated to dryness and the residue purified by column chromatography on silica (Merck "Kieselgel 60"--Trade Mark) (2 passes) eluting primarily with ethyl acetate:diethylamine 97:3 and, secondly, dichloromethane: methanol 97:3. The product-containing fractions were evaporated to dryness, the residue re-dissolved in 2 cm3 dichloromethane, and the required solid precipitated by the addition of 25 cm3 ether, yield 0.35 g (16%), m.p. 124°-127°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04904671
Source datasetuspto-grants-1990_02
ORD IDord-acea7259ccad40e2a8f00f5aeaeba4f0
Source noteuspto-grants-1990_02