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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81014Generated: October 28, 2026

2-Methylphenyl boronic acid → HCID 86665677, compound

https://huagongshe.com/reaction/81014

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylphenyl boronic acidHCID 2733267—
Reactant2-Chloro-6-cyclopentyl-4-(4-hydroxyphenyl)nicotinonitrileHCID 136372347—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
ProductHCID 86665677HCID 8666567758%

Reaction Steps

A mixture of 2-chloro-6-cyclopentyl-4-(4-hydroxyphenyl)nicotinonitrile (20 mg, 0.067 mmol, product A from Step 4 of Example 2), o-tolylboronic acid (36.4 mg, 0.268 mmol), copper(II) acetate (14.59 mg, 0.080 mmol) and 4 A molecular sieves (100 mg) in dichloromethane (3 mL) was stirred at room temperature while opening to the air for 40 h. The mixture was filtered through a CELITE® pad and the pad rinsed with ethyl acetate (50 mL). The filtrate was washed with saturated sodium bicarbonate (5 mL), water (5 mL), brine (5 mL), dried (MgSO4) and concentrated. Silica gel chromatography, eluting with 0-15% ethyl acetate in hexanes, gave 2-chloro-6-cyclopentyl-4-(4-(o-tolyloxy)phenyl)nicotinonitrile as a colorless liquid (15 mg, 58% yield). 1H NMR (400 MHz, CDCl3) δ ppm 7.50 (2H, δ, J=8.53 Hz), 7.07-7.32 (5H, m), 6.91-7.03 (2H, m), 3.05-3.28 (1H, m), 2.20 (3H, s), 1.98-2.13 (2H, m), 1.60-1.91 (6H, m); MS (ES+) m/z: 389 (M+H); LC retention time: 4.578 min (analytical HPLC Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846673B2
Source datasetuspto-grants-2014_09
ORD IDord-21b0a40c892b4bd68d56e7b53cf0c117
Source noteuspto-grants-2014_09