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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965800Generated: October 31, 2026

Diethyl Pyrocarbonate → Tert-butyl 4-({[(5-amino-6-chloro-2-ethylimidazo[1,2-a]pyridin-8-yl)carbonyl]amino}methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/965800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl PyrocarbonateHCID 3051—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
Reactant5-Amino-6-chloro-2-ethylimidazo[1,2-a]pyridine-8-carboxylic acidHCID 22236496—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-({[(5-amino-6-chloro-2-ethylimidazo[1,2-a]pyridin-8-yl)carbonyl]amino}methyl)piperidine-1-carboxylateHCID 2223650290%

Reaction Steps

A mixture of 5-amino-6-chloro-2-ethylimidazo[1,2-a]pyridine-8-carboxylic acid (Example 4, 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), DEPC (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 numberUS06951867B2
Source datasetuspto-grants-2005_10
ORD IDord-596ddcdc5866481d803d4f6ad3a73b91
Source noteuspto-grants-2005_10