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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661632Generated: October 29, 2026

Methyl iodide → 2-(4-methoxy-pyridin-3-yl)-1-methyl-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/1661632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(4-methoxy-pyridin-3-yl)-1H-indole-5-carbonitrileHCID 58215634—
SolventDimethylformamideHCID 6228—
Product2-(4-methoxy-pyridin-3-yl)-1-methyl-1H-indole-5-carbonitrileHCID 58215718—

Reaction Steps

To a solution of 2-(4-methoxy-pyridin-3-yl)-1H-indole-5-carbonitrile (Example 90, 178 mg, 0.649 mmol) in DMF (4 mL) is added 60% sodium hydride in mineral oil (78 mg, 1.95 mmol) and the suspension is stirred for 30 min. Iodomethane (138 mg, 0.97 mmol) is then added to the reaction mixture which is stirred at ambient temperature for 1 h. Aqueous NaHCO3 (3 mL) is added to quench the reaction and the mixture is filtered and purified by HPLC using an Xbridge C18 with a gradient of acetonitrile in 0.1% NH4OH to afford 2-(4-methoxy-pyridin-3-yl)-1-methyl-1H-indole-5-carbonitrile as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 3.59 (s, 3H), 3.89 (s, 3H), 6.67 (s, 1H), 7.27 (d, J=5.8 Hz, 1H), 7.54 (dd, J=8.6, 1.5 Hz, 1H), 7.70 (d, J=8.6 Hz, 1H), 8.11 (d, J=1.1 Hz, 1H), 8.42 (s, 1H), 8.60 (d, J=5.8 Hz, 1H). HRMS (ESI) m/z 264.1138 [(M+H)+ calcd for C16H14N3O: 264.1137].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030334B2
Source datasetuspto-grants-2011_10
ORD IDord-07a7aaf84c13416a9725e5f010236136
Source noteuspto-grants-2011_10