Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21217Generated: October 26, 2026

Water → 4-Vinyl-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone

https://huagongshe.com/reaction/21217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4,6-Trivinylboroxin-Pyridine ComplexHCID 2734806—
Reactant4-Trifluoromethanesulfonyloxy-7-(1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinoneHCID 86628286—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-Vinyl-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinoneHCID 6849248667%

Reaction Steps

In a similar manner to Step 1 of Example 152, 4-trifluoromethanesulfonyloxy-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone (60.0 mg, 0.114 mmol) was dissolved in dimethoxyethane (3.0 mL), and the solution was treated with 2,4,6-trivinylcyclotriboroxane-pyridine complex (55.0 mg, 0.228 mmol), [bis(diphenylphosphino)ferrocene]dichloropalladium (7.4 mg, 0.0091 mmol), potassium carbonate (79 mg, 0.57 mmol) and water (0.041 mL), followed by purification by preparative thin-layer chromatography (chloroform/methanol=8/1) to obtain 4-vinyl-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone (36.0 mg, yield 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-46db3b00ed554e74822bc260c80677a0
Source noteuspto-grants-2010_06