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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622344Generated: October 31, 2026

4-Methoxybenzaldehyde → HCID 45275023, compound

https://huagongshe.com/reaction/1622344

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 45275021HCID 45275021—
SolventMethanolHCID 887—
ProductHCID 45275023HCID 4527502319%

Reaction Steps

To a solution of N-(2-aminoethyl)-1-(3,5-dichloropyridin-4-yl)piperidine-4-carboxamide E13 (50 mg, 0.16 mmol) in MeOH (5 mL) was added anisaldehyde (19 μL, 0.16 mmol). After stirring for 2 h, sodium cyanoborohydride (20 mg, 0.32 mmol) was added and the mixture was stirred for a further 20 h. The solvent was removed under reduced pressure, the residue was dissolved in EtOAc (20 mL), washed with a saturated solution of sodium hydrogencarbonate (25 mL), brine (25 mL), dried (MgSO4) and the solvent was removed under reduced pressure. The crude product was purified by preparative tlc on silica gel (CH2Cl2, MeOH, 9:1) to furnish the title compound as a colourless oil (13 mg, 19%), umax (CHCl3)/cm−1 3008, 2839, 1660, 1513, 1249, 1174, 1036; m/z (ESI) C21H27Cl2N4O2 requires 437.1506, found [M+H]+ 437.1508.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778925B2
Source datasetuspto-grants-2014_07
ORD IDord-db0d5f9b229740e3a57a68ff96f332f6
Source noteuspto-grants-2014_07