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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743813Generated: October 30, 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/1743813

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 3, 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 numberUS07012080B2
Source datasetuspto-grants-2006_03
ORD IDord-9c9cbd322a46431c8aa3778a6cfc37cb
Source noteuspto-grants-2006_03