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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213679Generated: October 25, 2026

Piperidine → 5-Cyano-3-[1-(pyrrol-2-yl)ethylidene]indolin-2-one

https://huagongshe.com/reaction/2213679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant2-AcetylpyrroleHCID 14079—
Reactant2-Oxo-2,3-dihydro-1H-indole-5-carbonitrileHCID 2773346—
SolventEthanolHCID 702—
Product5-Cyano-3-[1-(pyrrol-2-yl)ethylidene]indolin-2-oneHCID 69545231—

Reaction Steps

To a suspension of 5-cyanoindolin-2-one (158 mg, 1 mmol) in ethanol (15 mL) was added 2-acetylpyrrole (95 mg, 1 mmol) and piperidine (0.1 mL). The reaction mixture was refluxed for 2 hours. A golden-colored product precipitated from the reaction mixture, which was filtered and washed with ethanol to afford 5-cyano-3-[1-(pyrrol-2-yl)ethylidene]indolin-2-one; (160 mg) 1H NMR (400 MHz, DMSO-d6) δ 2.80 (s, 3H), 6.40. (m, 1H), 7.04 (d, 1H), 7.20 (m, 1H), 7.42 (m, 1H), 7.60 (dd, 1H), 8.04 (s, 1H), 11.40 (s, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105563B2
Source datasetuspto-grants-2006_09
ORD IDord-b24a7961fea84a1cbb0f94b2e807fcc6
Source noteuspto-grants-2006_09