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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743824Generated: November 1, 2026

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

https://huagongshe.com/reaction/1743824

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
ReactantMethyl 5-amino-6-chloro-2-methylimidazo[1,2-a]pyridine-8-carboxylic acidHCID 67550158—
ProductTert-butyl 4-({[(5-amino-6-chloro-2-methylimidazo[1,2-a]pyridin-8-yl)carbonyl]amino}methyl)piperidine-1-carboxylateHCID 22236490—

Reaction Steps

The title compound was prepared, according to the procedure described in the step 6 of EXAMPLE 1, from 5-amino-6-chloro-2-methylimidazo[1,2-a]pyridine-8-carboxylic acid (EXAMPLE 1, Step 5) and tert-butyl 4-(aminomethyl)piperidine-1-carboxylate (J. Prugh, L. A. Birchenough and M. S. Egbertson, Synth. Commun., 1992, 22, 2357–60).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012080B2
Source datasetuspto-grants-2006_03
ORD IDord-185bc7c765d44b8894f0dd30b46b4d31
Source noteuspto-grants-2006_03