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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292985Generated: October 30, 2026

Pyridine → HCID 68851274, compound

https://huagongshe.com/reaction/1292985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 178486924HCID 178486924—
CatalystCupric acetateHCID 8895—
ProductHCID 68851274HCID 6885127425%

Reaction Steps

A mixture of 5-(4-benzylpiperazin-1-yl)-6-methoxy-3-(phenylsulfonyl)-1H-indazole (448 mg, 0.97 mmol), phenylboronic acid (242 mg, 1.94 mmol), copper(II) acetate (271 mg, 1.50 mmol), pyridine (160 mg, 2.00 mmol) and 4 Å molecular sieves (1.0 g) in methylene chloride is stirred at room temperature for 48 h and filtered. The filtercake is washed with THF. The filtrates are combined and concentrated in vacuo. The resultant residue is chromatographed (silica gel, 60:40 and 80:20 ethyl acetate:hexanes as eluents) to afford the free amine of the title product as a white solid, 130 mg (25% yield). The free amine is dissolved in ethanol, treated with 4.0 M HCl in dioxane, and concentrated in vacuo to a solid residue. This solid is triturated with ethyl acetate to afford the title product as a white solid, mp: 210–212° C., identified by NMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238696B2
Source datasetuspto-grants-2007_07
ORD IDord-5a421678a8cc4cf0b376abeaf047e459
Source noteuspto-grants-2007_07