HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199985Generated: October 31, 2026
2-Chlorobenzaldehyde → HCID 131716322, compound
https://huagongshe.com/reaction/1199985
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | 3-Oxo-3-phenyl-N-(pyridin-2-yl)propanimidic acid | HCID 268038 | — |
| Reactant | HCID 70357192 | HCID 70357192 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131716322 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04904671 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-acea7259ccad40e2a8f00f5aeaeba4f0 |
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| Source note | uspto-grants-1990_02 |
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