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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Bromo-7-methyl-2-(4-phenoxybenzyl)-2,3-dihydroisoindol-1-one | HCID 11603900 | — |
| Reactant | 1-Methyl-4-(prop-2-yn-1-yl)piperazine | HCID 13514091 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Diisopropylamine | HCID 7912 | — |
| Product | HCID 57949495 | HCID 57949495 | 43% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968570B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-d74daebc7a2046ae992599d7326e56c9 |
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| Source note | uspto-grants-2011_06 |
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