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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501071Generated: October 26, 2026

Acetic Acid → 4-Amino-3-[(1-benzylpiperidin-4-yl)amino)pyridine

https://huagongshe.com/reaction/501071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3,4-DiaminopyridineHCID 5918—
Reactant1-Benzyl-4-piperidoneHCID 19220—
Solvent1,1-DichloroethaneHCID 6365—
Product4-Amino-3-[(1-benzylpiperidin-4-yl)amino)pyridineHCID 2229324598.2%

Reaction Steps

A mixture of 3,4-diaminopyridine (1.1 g, 10.1 mmol), 1-benzyl-4-piperidone (3.2 g, 16.9 mmol) sodium triacetoxyborohydride (4.0 g, 18.9 mmol), and acetic acid (10.7 mL) in dichloroethane (10 mL) was stirred for about 6 days at room temperature. The reaction was concentrated to near dryness, and partitioned between chloroform (5×50 mL) and 1N sodium hydroxide (50 mL). The organic phase was dried over magnesium sulfate and concentrated to give the title compound (2.8 g). MS 283 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772224B2
Source datasetuspto-grants-2010_08
ORD IDord-86dec71c94154496ae785bd3b72cf881
Source noteuspto-grants-2010_08