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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766477Generated: October 31, 2026

4-Chlorophenylboronic acid → 5-(4-chloro-phenyl)-6-cyclobutylmethoxy-N-((1R,2R)-2-hydroxy-cyclohexyl)-nicotinamide

https://huagongshe.com/reaction/1766477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorophenylboronic acidHCID 74299—
ReactantCyclobutylcarbinolHCID 78130—
Reactant5-Bromo-6-chloropyridine-3-carboxylic acidHCID 285433—
ReactantCyclohexanol, 2-amino-, hydrochloride (1:1), (1R,2R)-HCID 12228412—
Product5-(4-chloro-phenyl)-6-cyclobutylmethoxy-N-((1R,2R)-2-hydroxy-cyclohexyl)-nicotinamideHCID 11952019—

Reaction Steps

The title compound was synthesized in analogy to Example 75, using 5-bromo-6-chloro-3-pyridinecarboxylic acid, cyclobutanemethanol, (4-chloro-phenyl)-boronic acid and (1R,2R)-2-amino-cyclohexanol hydrochloride as starting materials to yield 5-(4-chloro-phenyl)-6-cyclobutylmethoxy-N-((1R,2R)-2-hydroxy-cyclohexyl)-nicotinamide. MS (ISP) 415.4 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07229999B2
Source datasetuspto-grants-2007_06
ORD IDord-3818748c2522436c98ba7f7171dca600
Source noteuspto-grants-2007_06