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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518325Generated: October 31, 2026

Methyl iodide → HCID 118022858, compound

https://huagongshe.com/reaction/518325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 118022092HCID 118022092—
SolventDimethylformamideHCID 6228—
ProductHCID 118022858HCID 11802285876.5%

Reaction Steps

To a solution of tert-butyl N-(5-bromo-1-methyl-2-oxopyridin-3-yl)carbamate (150.0 mg, impure) in DMF (10 mL) was added NaH (60.0 mg, 1.5 mol, 60% in oil) in portions at 0° C. It was stirred for 30 min. Then CH3I (231.0 mg, 1.5 mmol) was added dropwise at 0° C. The reaction mixture was stirred for 2 h at 30° C. The reaction was quenched with saturated aqueous NH4Cl (15 mL), extracted with EA (20 mL), washed with brine (20 mL), dried over Na2SO4, filtered and concentrated to give the title compound (120.0 mg, crude) as a green solid, which was used directly in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115114B2
Source datasetuspto-grants-2015_08
ORD IDord-bce5bdf9b06d433daf60abe69d5ae6a6
Source noteuspto-grants-2015_08