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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859068Generated: October 31, 2026

Piperidine → (Z)-1,3-Dihydro4-fluoro-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-5-nitro-2H-indol-2-one

https://huagongshe.com/reaction/1859068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantEthyl AcetateHCID 8857—
Reactant1H-Pyrrole-2-carboxaldehyde, 3-methoxy-HCID 11286466—
Reactant4-Fluoro-5-nitroindolin-2-oneHCID 15512600—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product(Z)-1,3-Dihydro4-fluoro-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-5-nitro-2H-indol-2-oneHCID 15512601—

Reaction Steps

1,3-Dihydro-4-fluoro-5-nitro-2H-indol-2-one (5.25 g, 26.8 mmol) (Starting Material 9) was suspended in 110 mL solution of 1.35% piperidine in 2-propanol (Aldrich). 3-Methoxy-2-pyrrolecarboxaldehyde (3.68 g, 29.4 mmol, 1.1 eq.)(Bellamy, supra) was added and this mixture heated at 60° C. for 3.5 hours (TLC: 50% ethyl acetate in hexanes). The reaction mixture was poured into 1 L ice and water mixture and the solid precipitate filtered, washed with water and dried at 50° C. under high vacuum to give (Z)-1,3-dihydro-4-fluoro-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-5-nitro-2H-indol-2-one as an orange-brown solid. (Yield 6.6 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06153634
Source datasetuspto-grants-2000_11
ORD IDord-acf5040a3ee5452db029b08e7146b024
Source noteuspto-grants-2000_11