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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420600Generated: November 1, 2026

4-Pyridinecarboxaldehyde → HCID 18612944, compound

https://huagongshe.com/reaction/1420600

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinecarboxaldehydeHCID 13389—
ReactantMethyl [(2-aminobenzyl)-(4-methoxybenzenesulfonyl)amino]-3-hydroxypropionateHCID 18612758—
SolventEthanolHCID 702—
ProductHCID 18612944HCID 1861294465.2%

Reaction Steps

A mixture of 0.50 g (1.268 mmol) of methyl 2-[(2-aminobenzyl)-(4-methoxybenzenesulfonyl)amino]-3-hydroxypropionate and 1.268 mmol of 4-pyridinecarboxaldehyde in 7 ml of anhydrous ethanol was refluxed for 1.5 hours and the mixture concentrated under vacuum to dryness. To the residue was added H2O and ethyl acetate. The ethyl acetate layer was separated and concentrated to dryness under vacuum. The solid was purified by thick layer chromatography on silica gel with hexane-ethyl acetate as solvent to give 0.40 g of solid product (plus a small amount of starting material). Anal. for C24H25N3O6S: Calc'd: C,59.6; H,5.2; N,8.7; Found: C,57.6; H,5.7; N,7.4; Mass spectrum (ES) 484 (M+H)-product; 395.1 (M+H)-starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071903
Source datasetuspto-grants-2000_06
ORD IDord-70e83fa32f9a4f0ab6041a2c0146ff06
Source noteuspto-grants-2000_06