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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662737Generated: October 25, 2026

5-chloro-1H-indole-2,3-dione → 5-chloro-3-hydroxy-3-(2-methoxy-5-morpholin-4-ylphenyl)-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/1662737

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-chloro-1H-indole-2,3-dioneHCID 87203—
Reactant4-(3-Bromo-4-methoxyphenyl)morpholineHCID 67429791—
Product5-chloro-3-hydroxy-3-(2-methoxy-5-morpholin-4-ylphenyl)-1,3-dihydro-2H-indol-2-oneHCID 6742890977.3%

Reaction Steps

With 2.00 g of the compound obtained in Step 191-1 and 953 mg of 5-chloroisatin as starting materials, 1.52 g of the title compound (pale yellow amorphous) was obtained by a similar method to Step 21-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030499B2
Source datasetuspto-grants-2011_10
ORD IDord-4295049017c74788805de3e2f81f0b14
Source noteuspto-grants-2011_10