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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159282Generated: November 1, 2026

4-Chlorophenylboronic acid → 5-(4-chloro-phenyl)-N-((R)-2-cyclopropyl-2-hydroxy-propyl)-6-(3-methyl-isoxazol-5-ylmethoxy)-nicotinamide

https://huagongshe.com/reaction/1159282

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant5-Bromo-6-chloropyridine-3-carboxylic acidHCID 285433—
Reactant(3-Methylisoxazol-5-yl)methanolHCID 10820493—
Reactant(2R)-1-amino-2-cyclopropyl-propan-2-olHCID 51684102—
Product5-(4-chloro-phenyl)-N-((R)-2-cyclopropyl-2-hydroxy-propyl)-6-(3-methyl-isoxazol-5-ylmethoxy)-nicotinamideHCID 24856638—

Reaction Steps

The title compound was synthesized in analogy to Example 31, using 5-bromo-6-chloro-3-pyridinecarboxylic acid, 3-methyl-5-isoxazolemethanol, (4-chloro-phenyl)-boronic acid and (R)-α-(aminomethyl)-α-methyl-cyclopropanemethanol as starting materials to yield 5-(4-chloro-phenyl)-N—((R)-2-cyclopropyl-2-hydroxy-propyl)-6-(3-methyl-isoxazol-5-ylmethoxy)-nicotinamide as a white foam, MS (ISP) 442.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812028B2
Source datasetuspto-grants-2010_10
ORD IDord-6c1ca25e76e844789e5b289278dc5eee
Source noteuspto-grants-2010_10