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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622346Generated: October 31, 2026

Benzaldehyde → HCID 45275133, compound

https://huagongshe.com/reaction/1622346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 45275021HCID 45275021—
SolventMethanolHCID 887—
ProductHCID 45275133HCID 4527513354%

Reaction Steps

To a solution of N-(2-aminoethyl)-1-(3,5-dichloropyridin-4-yl)piperidine-4-carboxamide E13 (20 mg, 0.060 mmol) in MeOH (2 mL) was added benzaldehyde (19 μL, 0.19 mmol). After stirring for 45 min, sodium cyanoborohydride (12 mg, 0.19 mmol) was added and the mixture was stirred for a further 16 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 white solid (14 mg, 54%), m.p. 147-149° C.; umax (CHCl3)/cm−1 3007, 2837, 1658, 1558, 1509, 1457, 1146; m/z (ESI) C27H31Cl2N4O requires 497.1869, found [M+H]+ 497.1872.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778925B2
Source datasetuspto-grants-2014_07
ORD IDord-68acebd68e70468290d6f31bfb763f20
Source noteuspto-grants-2014_07