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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588389Generated: October 30, 2026

(R)-tert-butyl 3-((3-chloropyridin-2-yl)amino)piperidine-1-carboxylate → tert-butyl (3R)-3-[(3-chloropyridin-2-yl){[5-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)pyridin-2-yl]carbonyl}amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/588389

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-tert-butyl 3-((3-chloropyridin-2-yl)amino)piperidine-1-carboxylateHCID 117652951—
Reactant5-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)pyridine-2-carboxylic acidHCID 117653100—
Producttert-butyl (3R)-3-[(3-chloropyridin-2-yl){[5-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)pyridin-2-yl]carbonyl}amino]piperidine-1-carboxylateHCID 11889860052%

Reaction Steps

Prepared using General Procedures A and C starting from Preparation 1 tert-butyl (3R)-3-[(3-chloropyridin-2-yl)amino]piperidine-1-carboxylate (3.22 g, 10.3 mmol) and Preparation 7 5-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)pyridine-2-carboxylic acid (2.37 g, 9.83 mmol) to provide 2.72 g (52%) of the product isolated as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227956B2
Source datasetuspto-grants-2016_01
ORD IDord-078368856e5e4ccaad2c68185d841fe7
Source noteuspto-grants-2016_01