Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24515Generated: October 26, 2026

6-(3-Methoxyphenyl)-1,3-dihydroindol-2-one → 3-(2-[6-(3-methoxyphenyl)-2-oxo-1,2-dihydroindol-3-ylidenemethyl]-4,5,6,7-tetrahydro-1H-indol-3-yl}-propionic acid

https://huagongshe.com/reaction/24515

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(3-Methoxyphenyl)-1,3-dihydroindol-2-oneHCID 10586070—
Reactant3-(2-formyl-4,5,6,7-tetrahydro-1H-indol-3-yl)propionic acidHCID 10609002—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Product3-(2-[6-(3-methoxyphenyl)-2-oxo-1,2-dihydroindol-3-ylidenemethyl]-4,5,6,7-tetrahydro-1H-indol-3-yl}-propionic acidHCID 5381977082.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 103 mg 6-(3-methoxyphenyl)-2-oxindole, 95 mg 3-(2-formyl-4,5,6,7-tetrahydro-1H-indol-3-yl)-propionic acid and piperidine (3 drops) in ethanol (2 mL) was heated in sealed tube to 90° C. and held there overnight. The reaction mixture was concentrated and acidified with 6 N hydrochloric acid. The precipitate that formed was collected by filtration and washed with water and hexane to give 156 mg of 3-{2-[6-(3-methoxyphenyl)-2-oxo-1,2-dihydroindol-3-ylidenemethyl]-4,5,6,7-tetrahydro-1H-indol-3-yl}-propionic acid as a brown solid (82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855730B2
Source datasetuspto-grants-2005_02
ORD IDord-fdeb87ac291640ef98ee2b47813e3d0e
Source noteuspto-grants-2005_02