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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623502Generated: November 2, 2026

2H-Indol-2-one, 5-(4-ethenyl-3-pyridinyl)-1,3-dihydro-1-methyl- → HCID 66788362, compound

https://huagongshe.com/reaction/1623502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2H-Indol-2-one, 5-(4-ethenyl-3-pyridinyl)-1,3-dihydro-1-methyl-HCID 66793926—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 66788362HCID 66788362—

Reaction Steps

To a solution of 1-methyl-5-(4-vinyl-pyridin-3-yl)-1,3-dihydro-indol-2-one (30 mg, 0.12 mmol) in ethanol (1 mL) was added 10% palladium on carbon (18 mg, 0.02 mmol). The atmosphere over the reaction mixture was evacuated and the reaction was placed under an atmosphere of hydrogen gas via a balloon. The reaction was stirred for 25 minutes. The reaction mixture was then filtered through a plug of Celite® and the filtrate was then concentrated to dryness. The resulting residue was purified by silica gel flash chromatography (ethanol-dichloromethane, 0 to 6%) to afford 5-(4-ethyl-pyridin-3-yl)-1-methyl-1,3-dihydro-indol-2-one. The HCl salt of the title compound was prepared by dissolution in diethyl ether followed by treatment with an excess of 1N HCl in diethyl ether. The resulting heterogeneous solution was concentrated to furnish the HCl salt of 5-(4-ethyl-pyridin-3-yl)-1-methyl-1,3-dihydro-indol-2-one. HRMS: (ESI) m/z 253.1335 (M+H)+; 1H NMR (400 MHz, CD3OD) δ ppm 1.23 (t, J=7.6 Hz, 3H), 2.93 (q, J=7.6 Hz, 2H), 3.28 (s, 3H), 3.66 (s, 2H), 7.16 (d, J=8.6 Hz, 1H), 7.33-7.43 (m, 2H), 8.05 (d, J=6.3 Hz, 1H), 8.65 (s, 1H), 8.71 (d, J=6.1 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778972B2
Source datasetuspto-grants-2014_07
ORD IDord-7a3187a14b3d417991560d58243aad2b
Source noteuspto-grants-2014_07