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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382737Generated: October 31, 2026

HCID 54056370, compound → HCID 18360792, compound

https://huagongshe.com/reaction/382737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54056370HCID 54056370—
ReactantHCID 70032616HCID 70032616—
SolventEthanolHCID 702—
ProductHCID 18360792HCID 18360792—

Reaction Steps

A solution of 2-[(4-nitrophenyl)methylene]-3-oxohexanoic acid 2-cyanoethyl ester (9.80 g, 30 mmol) and benzyl 3-amino-2-hexenoate (7.24 g, 33 mmol) in 150 ml of EtOH was refluxed for 36 hrs. After the solvent was removed in vacuo, the residue was dissolved in 250 ml of CHCl3, washed with water (2×100 ml) and dried over Na2SO4. After filtration and evaporation of solvent, 5-benzyloxycarbonyl-3-(2-cyanoethoxy)carbonyl-1,4-dihydro-4-(4-nitrophenyl)-2,6-dipropylpyridine was obtained as a yellow oil (15.4 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310076B1
Source datasetuspto-grants-2001_10
ORD IDord-216ac884eed54a209934df7f7876f24b
Source noteuspto-grants-2001_10