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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489810Generated: October 31, 2026

Dimethylamine, hydrochloride → 6-Amino-5-chloro-N-[(1-{1-[(dimethylamino)carbonyl]pentyl}piperidin-4-yl)methyl]-2-methoxynicotinamide

https://huagongshe.com/reaction/489810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantDiethyl cyanophosphonateHCID 76257—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-[4-({[(6-Amino-5-chloro-2-methoxypyridin-3-yl)carbonyl]amino}-methyl)piperidine-1-yl]hexanoic acidHCID 22262663—
SolventDimethylformamideHCID 6228—
Product6-Amino-5-chloro-N-[(1-{1-[(dimethylamino)carbonyl]pentyl}piperidin-4-yl)methyl]-2-methoxynicotinamideHCID 2226262710.4%

Reaction Steps

To a solution of 2-[4-({[(6-amino-5-chloro-2-methoxypyridin-3-yl)carbonyl]amino}methyl)piperidine-1-yl]hexanoic acid (500 mg, 1.2 mmol) in dimethylformamide (30 ml) was added diethyl cyanophosphonate (300 mg, 1.8 mmol), N,N-dimethylamine hydrochloride (148 mg, 1.8 mmol) and N,N-diisopropylethylamine (0.63 ml, 3.6 mmol). The mixture was stirred for 72 h at room temperature. The mixture was concentrated in vacuo. The resultant amorphous solid was chromatographed on a column of silica gel eluting with dichloromethane/methanol (20:1) to give 55 mg (10%) of the title compound as a colorless amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979690B2
Source datasetuspto-grants-2005_12
ORD IDord-0919433952e64065a69684769001064b
Source noteuspto-grants-2005_12