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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445611Generated: October 31, 2026

Methyl iodide → N-(5-Bromo-2-methoxy-pyridin-3-yl)-N-methyl-acetamide

https://huagongshe.com/reaction/445611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantN-(5-bromo-2-methoxypyridin-3-yl)acetamideHCID 59619883—
SolventDimethylformamideHCID 6228—
ProductN-(5-Bromo-2-methoxy-pyridin-3-yl)-N-methyl-acetamideHCID 59619892—

Reaction Steps

To N-(5-bromo-2-methoxy-pyridin-3-yl)-acetamide (Stage 62.1.3, 100 mg, 0.408 mmol) DMF (1 ml) was added NaH 55% in oil (19.6 mg, 0.45 mmol). The reaction mixture was stirred for 10 min at rt then was added MeI (0.031 ml, 0.49 mmol). The reaction mixture was stirred for 1 h at rt then quenched with brine and extracted with EtOAc (2×). The organic layers are washed with brine (3×), dried over Na2SO4, filtered and evaporated. The crude product was purified by Prep.HPLC. The fractions containing the product were collected together and basified with NaHCO3, before being concentrated and extracted with EtOAc (3×). The organic layers were dried over Na2SO4, filtered and evaporated to dryness to give the title compound as an off-white solid (HPLC: tR 2.75 min (Method A); M+H=259, 261 MS-ES).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476294B2
Source datasetuspto-grants-2013_07
ORD IDord-81934f1f76014f1a923ae8b1fb27f761
Source noteuspto-grants-2013_07