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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240233Generated: October 30, 2026

Methyl iodide → 1-Methyl-4-nitro-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/2240233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-Nitro-7-azaindoleHCID 639248—
SolventDimethylacetamideHCID 31374—
Product1-Methyl-4-nitro-1H-pyrrolo[2,3-b]pyridineHCID 59305025—

Reaction Steps

170 mg (4.29 mmol) of sodium hydride are added to a solution of 500 mg (3.06 mmol) of 4-nitro-1H-pyrrolo[2,3-b]pyridine (Antonini, Ippolito; Claudi, Francesco; Cristalli, Gloria; Franchetti, Palmarisa; Grifantini, Mario; Martelli, Sante; J. Med. Chem. 1982, 25, 1258-1261.) in 10 ml of absolute DMA, and the suspension is stirred for 30 min. A solution of 230 μl (3.68 mmol) of methyl iodide in 2 ml of absolute DMA is then slowly added dropwise, and the mixture is again stirred for 60 min. After concentration under reduced pressure, the residue is purified by column chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 10:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723347B2
Source datasetuspto-grants-2010_05
ORD IDord-98480131891e46e5906bc224961c01e5
Source noteuspto-grants-2010_05