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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829002Generated: October 27, 2026

3-Bromo-1-propanol → 3-[6-(3-Hydroxy-propylamino)-3H-isobenzofuran-1-ylidene]-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1829002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-1-propanolHCID 12308—
Reactant3-(6-Amino-2-benzofuran-1(3H)-ylidene)-1,3-dihydro-2H-indol-2-oneHCID 69659199—
CatalystHCID 178418844HCID 178418844—
SolventDimethylformamideHCID 6228—
Product3-[6-(3-Hydroxy-propylamino)-3H-isobenzofuran-1-ylidene]-1,3-dihydro-indol-2-oneHCID 6965962110%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3-(6-Amino-3H-isobenzofuran-1-ylidene)-1,3-dihydro-indol-2-one (25.0 mg, 0.095 mmol), 3-bromo-1-propanol (85.5 μL, 0.946 mmol), and silver sulfate (59.0 mg, 0.189 mmol) in 0.8 mL DMF was heated at 120° C. for 1.5 h. The mixture was partitioned between EtOAc and H2O and the organic layer separated from the silver salts. The solution was washed with H2O, brine and then dried with Na2SO4. Concentrating the solution in vacuo gave a residue which was purified by chromatography (silica gel, CHCl3/MeOH, 96:4) to give the title compound (3 mg, 10%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060844B2
Source datasetuspto-grants-2006_06
ORD IDord-6280d3cc889e4898ab37b0a83799022a
Source noteuspto-grants-2006_06