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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427694Generated: October 30, 2026

5-Bromo-7-methyl-2-(4-phenoxybenzyl)-2,3-dihydroisoindol-1-one → HCID 57949495, compound

https://huagongshe.com/reaction/2427694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-7-methyl-2-(4-phenoxybenzyl)-2,3-dihydroisoindol-1-oneHCID 11603900—
Reactant1-Methyl-4-(prop-2-yn-1-yl)piperazineHCID 13514091—
ReactantChloroform methanolHCID 21584188—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDiisopropylamineHCID 7912—
ProductHCID 57949495HCID 5794949543%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-methyl-4-prop-2-ynyl-piperazine (0.033 mL, 0.33 mmol), 5-bromo-7-methyl-2-(4-phenoxy-benzyl)-2,3-dihydro-isoindol-1-one (0.102 g, 0.25 mmol), PdCl2(PPh3)2 (0.011 g, 0.015 mmol), and CuI (0.0028 g, 0.015 mmol) in diisopropyl amine (4 mL) was stirred at 100° C. for 2 h. Workup and silica gel column chromatography using 10:1 CHCl3-MeOH afforded 7-methyl-5-[3-(4-methyl-piperazin-1-yl)-prop-1-ynyl)-2-(4-phenoxy-benzyl)-2,3-dihydro-isoindol-1-one (0.05 g, 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968570B2
Source datasetuspto-grants-2011_06
ORD IDord-d74daebc7a2046ae992599d7326e56c9
Source noteuspto-grants-2011_06