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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593561Generated: October 31, 2026

Methyl iodide → 1-methyl-2-pyridin-3-yl-1H-indole-3-carbonitrile

https://huagongshe.com/reaction/593561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
Reactant2-pyridin-3-yl-1H-indole-3-carbonitrileHCID 11447314—
SolventDimethylformamideHCID 6228—
Product1-methyl-2-pyridin-3-yl-1H-indole-3-carbonitrileHCID 58215779—

Reaction Steps

To 2-pyridin-3-yl-1H-indole-3-carbonitrile (1.0 g, 4.56 mmol) in DMF (17 mL) is added 60% sodium hydride in mineral oil (547 mg, 13.68 mmol) and the suspension is stirred for 30 min. Iodomethane (971 mg, 6.84 mmol) is then added to the reaction mixture and stirred at ambient temperature for 1 h. Aqueous NaHCO3 (3 mL) is added and the mixture is concentrated in vacuo. The residue is purified by purified by silica gel flash chromatography (dichloromethane-methanol gradient) to give 1-methyl-2-pyridin-3-yl-1H-indole-3-carbonitrile as a white solid. 1H NMR (400 MHz, MeOD) δ ppm 3.83 (s, 3H), 7.35 (t, J=7.5 Hz, 1H), 7.40-7.46 (m, 1H), 7.64 (d, J=8.3 Hz, 1H), 7.67-7.74 (m, 2H), 8.16 (dt, J=8.0, 2.0, 1.9 Hz, 1H), 8.76 (dd, J=5.1, 1.5 Hz, 1H), 8.86 (d, J=1.5 Hz, 1H). HRMS (ESI) m/z 234.1029 [(M+H)+ Calcd for C15H12N3: 234.1031].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242963B2
Source datasetuspto-grants-2016_01
ORD IDord-c1d9c39c248b465a8943ab1a19a7cc6a
Source noteuspto-grants-2016_01