Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492373Generated: October 30, 2026

1-Phenylpiperazine → HCID 59730369, compound

https://huagongshe.com/reaction/492373

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantSodium borohydrideHCID 4311764—
Reactant6-(4-Formylphenoxy)pyridine-3-carboxamideHCID 56851422—
SolventMethanolHCID 887—
ProductHCID 59730369HCID 5973036913%

Reaction Steps

Using a method similar to Example 334, using 6-(4-formyl-phenoxy)-nicotinamide (compound of example 332, step 1) (0.302 g, 1.25 mmol), 1-phenyl-piperazine (0.192 mL, 1.26 mmol), and sodium borohydride (0.110 g, 2.91 mmol) in methanol (12 mL) provides 0.0627 g (13%) of the title compound as a white solid Chromatography solvent: 25:1 methylene chloride:methanol. High resolution mass spectrum (electrospray): m/z calc for C23H25N4O2 389.1978, found 389.1993; 1H NMR (methanol-d4): 8.67 (d, 1H, J=2.0 Hz), 8.30 (dd, 1H, J=2.9, 8.8 Hz), 7.50 (d, 2H, J=8.8 Hz), 7.27 (dd, 2H, J=7.3, 8.8 Hz), 7.20-7.15 (m, 2H), 7.05 (d, 1H, J=8.3 Hz), 7.03-6.99 (m, 2H), 6.88 (t, 1H, J=7.3 Hz), 3.67 (s, 2H), 3.27-3.21 (m, 4H), 2.74-2.69 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531557B2
Source datasetuspto-grants-2009_05
ORD IDord-fae7b4b78b0940729ac498bc02bc6f83
Source noteuspto-grants-2009_05