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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382008Generated: October 27, 2026

Pyrrole-2-carboxaldehyde → (Z)-1,3-dihydro-4-iodo-3-[(1H-pyrrol-2-yl)methylene]-indol-2-one

https://huagongshe.com/reaction/382008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrole-2-carboxaldehydeHCID 13854—
Reactant4-Iodo-1,3-dihydro-2H-indol-2-oneHCID 10923225—
CatalystPiperidineHCID 8082—
SolventIsopropanolHCID 3776—
Product(Z)-1,3-dihydro-4-iodo-3-[(1H-pyrrol-2-yl)methylene]-indol-2-oneHCID 1554805265.2%

Reaction Conditions

Temperature23 °C

Reaction Steps

A mixture of 1,3-dihydro-4-iodo-2H-indol-2-one (404.1 mg, 1.56 mmol) (see Fukuyama et al., supra) and pyrrole-2-carboxaldehyde (163.2 mg, 1.72 mmol) (Aldrich) in 2-propanol (6.2 mL) was treated with 2 drops of piperidine. The reaction mixture was heated at reflux for 24 h and then allowed to cool to 23° C., at which time, the reaction mixture was filtered. The solid was washed several times with cold distilled water and then allowed to air dry to provide pure (Z)-1,3-dihydro-4-iodo-3-[(1H-pyrrol-2-yl)methylene]-2H-indol-2-one (341.8 mg, 65%) as a yellow solid which was used without further purification. (MP 256-258° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06307056B1
Source datasetuspto-grants-2001_10
ORD IDord-9c29a8266a2c433d9a43cbb3abbef0b1
Source noteuspto-grants-2001_10