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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726293Generated: October 31, 2026

3-Aminopyridine → Tert-butyl 4-[(pyridin-3-yl)amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/1726293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminopyridineHCID 10009—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ProductTert-butyl 4-[(pyridin-3-yl)amino]piperidine-1-carboxylateHCID 224994861,135.7%

Reaction Steps

Using general procedure A, 3-aminopyridine (1.43 g, 1.01 mmol) and 1-Boc-4-piperidone (3.0 g, 1.0 mmol) afforded 4-(pyridin-3-ylamino)-piperidine-1-carboxylic acid tert-butyl ester as a white solid (3.15 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491735B2
Source datasetuspto-grants-2009_02
ORD IDord-849614a11b37430284ee080817b85a1d
Source noteuspto-grants-2009_02