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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257057Generated: October 26, 2026

4-Phenoxybenzoyl chloride → N-[2-(6-Bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-1-cyano-1-methylethyl]-4-phenoxybenzamide

https://huagongshe.com/reaction/1257057

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenoxybenzoyl chlorideHCID 74193—
Reactant2-Amino-3-(6-bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-2-methylpropionitrileHCID 66620126—
SolventTetrahydrofuranHCID 8028—
ProductN-[2-(6-Bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-1-cyano-1-methylethyl]-4-phenoxybenzamideHCID 68706734—

Reaction Steps

Using a procedure similar to that described in Example 60, except using a solution of 4-phenoxybenzoyl chloride (0.16 mmole) in THF and a solution of 2-amino-3-(6-bromo-2H-pyrazolo[4,3-b]pyridin-2-yl)-2-methylpropionitrile (0.075 mmole, described in Example 182) in THF mixed with TEA (3% v./v.), the title compound was isolated as solid residue (6.7 mg). It was dissolved in DMSO for further biological evaluation and analyzed by LCMS. MS (ES): M/Z [M+H]=476, RT=0.63 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461176B2
Source datasetuspto-grants-2013_06
ORD IDord-527d0470645347c5a20398fb166ee7c0
Source noteuspto-grants-2013_06