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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168253Generated: November 1, 2026

Diethyl cyanophosphonate → 5-amino-6-chloro-2-ethyl-N-(piperidin-4-ylmethyl)imidazo[1,2-a]pyridine-8-carboxamide

https://huagongshe.com/reaction/1168253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl cyanophosphonateHCID 76257—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
Reactant5-Amino-6-chloro-2-ethylimidazo[1,2-a]pyridine-8-carboxylic acidHCID 22236496—
SolventDimethylformamideHCID 6228—
Product5-amino-6-chloro-2-ethyl-N-(piperidin-4-ylmethyl)imidazo[1,2-a]pyridine-8-carboxamideHCID 994961290%

Reaction Steps

A mixture of 5-amino-6-chloro-2-ethylimidazo[1,2-a]pyridine-8-carboxylic acid (EXAMPLE 10, Step 2, 10.00 g, 41.72 mmol), tert-butyl 4-(aminomethyl)piperidine-1-carboxylate (J. Prugh, L. A. Birchenough and M. S. Egbertson, Synth. Commun., 1992, 22, 2357-60) (15.20 g, 70.93 mmol), diethyl phosphorocyanidate (10.76 mL, 70.93 mmol) and diisopropylethylamine (18.17 mL, 104.4 mmol) in N,N-dimethylformamide (267 mL) was stirred at room temperature for 43 h. The solvent was removed by evaporation. The residue was basified with aqueous sodium bicarbonate (40 mL), and extracted with dichloromethane (5×100 mL). The combined extract was washed with brine, dried over magnesium sulfate, and concentrated in vacuo. Flash chromatography of the residue eluting with dichloromethane/methanol (100:1 to 20:1) afforded 19.08 g (90%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06624162B2
Source datasetuspto-grants-2003_09
ORD IDord-3d0e74c1d1c2417b8ded164c643c1665
Source noteuspto-grants-2003_09