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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512519Generated: October 27, 2026

6-(Bromomethyl)pyridine-3-carbonitrile → 1-(5-Cyano-pyridin-2-ylmethyl)-5-(3-difluoromethyl-phenyl)-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acid 4-methanesulfonyl-benzylamide

https://huagongshe.com/reaction/512519

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(Bromomethyl)pyridine-3-carbonitrileHCID 21927776—
Reactant5-(3-Difluoromethyl-phenyl)-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acid 4-methanesulfonyl-benzylamideHCID 86711567—
Product1-(5-Cyano-pyridin-2-ylmethyl)-5-(3-difluoromethyl-phenyl)-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acid 4-methanesulfonyl-benzylamideHCID 86711568—

Reaction Steps

Example 40 is prepared as described for example 2.1, substituting benzyl bromide with 6-bromomethyl-nicotinonitrile and substituting preparation 5 with preparation 39a. ESI mass spectrum: [M+H]+=563; Retention time HPLC: 0.99 min (Z018_S04).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102624B2
Source datasetuspto-grants-2015_08
ORD IDord-72bbe8dfcf944a0cbc2e31e692c0fc87
Source noteuspto-grants-2015_08