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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105009Generated: November 2, 2026

Pyridine → 4-((5-ethoxy-2-fluoro-3-isopropoxyphenyl)(1-phenyl-1H-pyrazol-3-yl)methylamino)benzonitrile

https://huagongshe.com/reaction/2105009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBoronic AcidHCID 61668—
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 178467025HCID 178467025—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product4-((5-ethoxy-2-fluoro-3-isopropoxyphenyl)(1-phenyl-1H-pyrazol-3-yl)methylamino)benzonitrileHCID 6881486771%

Reaction Steps

To a mixture of Intermediate 183.1 (39.5 mg, 0.100 mmol) and 3A molecular sieves (30 mg) in 1 mL CH2Cl2 at rt, was added TEA (0.028 mL, 0.20 mmol), pyridine (16 mg, 0.20 mmol) and phenylboronic acid (24.4 mg, 0.20 mmol). The mixture was stirred until the boronic acid dissolved, then Cu(OAc)2 (27.3 mg, 0.150 mmol) was added. The mixture was stirred for 5.5 h, then was diluted with EtOAc. The organic phase was washed with 0.5N HCl, H2O, sat. NaHCO3 and brine, dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography (0 to 50% EtOAc/hexanes gradient) to afford 33.4 mg of Intermediate 183.2 as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576098B2
Source datasetuspto-grants-2009_08
ORD IDord-298f58f917e640c2982473f620523590
Source noteuspto-grants-2009_08