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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228233Generated: October 30, 2026

Acetic Acid → HCID 59730115, compound

https://huagongshe.com/reaction/228233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-MethylpiperidineHCID 79081—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant6-(4-Formylphenoxy)pyridine-3-carboxamideHCID 56851422—
Solvent1,2-DichloroethaneHCID 11—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 59730115HCID 5973011529.5%

Reaction Steps

Using a method similar to Example 345, using 3-methyl-piperidine (0.0420 g, 0.423 mmol), 6-(4-formyl-phenoxy)-nicotinamide (compound of example 332, step 1) (0.101 g, 0.417 mmol), sodium triacetoxyborohydride (0.129 g, 0.610 mmol), and acetic acid (0.035 mL, 0.611 mmol) in 1,2-dichloroethane (8.0 mL) provides, after silica gel chromatography (10:1→7:3 methylene chloride:methanol), 0.0400 g (29%) of the title compound as a white foam: high resolution mass spectrum (electrospray): m/z calc for C19H24N3O2 326.1869, found 326.1841; 1H NMR (DMSO-d6): 8.66 (d, 1H, J=2.2 Hz), 8.29 (dd, 1H, J=2.5, 8.4 Hz), 8.06 (s b, 1H), 7.53 (s br, 1H), 7.38 (d, 2H, J=8.4 Hz), 7.17-7.09 (m, 3H), 3.38-3.28 (m, 2H), 2.83-2.70 (m, 2H), 1.95 (t, 1H, J=10.6 Hz), 1.74-1.41 (m, 5H), 0.97-0.79 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560463B2
Source datasetuspto-grants-2009_07
ORD IDord-8750c23c23a04349865924bc2cdd18e4
Source noteuspto-grants-2009_07