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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830833Generated: October 25, 2026

2-Phenylnicotinic acid → 2-Phenylpiperidin-3-amine

https://huagongshe.com/reaction/1830833

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Phenylnicotinic acidHCID 97489—
Reactant3-Amino-2-phenylpyridineHCID 2762784—
Product2-Phenylpiperidin-3-amineHCID 9794008—

Reaction Steps

First, a carboxyl group of a 2-phenylnicotinic acid derivative is amidated and applied to Hofmann's reaction. Then, the resulting 2-phenyl-3-aminopyridine derivative is reduced to produce a 2-phenyl-3-aminopiperidine derivative, and further subjecting the resulting compound to acylation or alkylation, if desired.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067535B2
Source datasetuspto-grants-2006_06
ORD IDord-d470a022d26b4b1aba454715856cc860
Source noteuspto-grants-2006_06