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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21092Generated: October 25, 2026

2-(Tributylstannyl)furan → 7-Amino-4-(furan-2-yl)isoindolinone

https://huagongshe.com/reaction/21092

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furanHCID 4393688—
Reactant7-Amino-4-bromo-2,3-dihydroisoindol-1-oneHCID 19701932—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product7-Amino-4-(furan-2-yl)isoindolinoneHCID 6849273955%

Reaction Steps

In a similar manner to Step 1 of Example 10, 7-amino-4-bromoisoindolinone (234 mg, 1.03 mmol) was dissolved in THF (11.6 mL), and the solution was treated with 2-(tributylstannyl)furane (0.649 mL, 2.06 mmol) and bis(triphenylphosphine)dichloropalladium (58 mg, 0.082 mmol), followed by purification by preparative thin-layer chromatography (chloroform/acetone=4/1, chloroform/methanol=12/1) to obtain 7-amino-4-(furan-2-yl)isoindolinone (121 mg, yield 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-68c7b12d71e149028aac55c12e0e9711
Source noteuspto-grants-2010_06