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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575596Generated: October 28, 2026

Methyl iodide → HCID 118022858, compound

https://huagongshe.com/reaction/575596

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 numberUS09034900B2
Source datasetuspto-grants-2015_05
ORD IDord-9b0b9678ca0a450c94d82d9404cf18e6
Source noteuspto-grants-2015_05