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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692762Generated: November 2, 2026

Methyl iodide → 2-(N-BOC-N-methylamino)-5-bromopyridine

https://huagongshe.com/reaction/1692762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
Reactant2-(Boc-amino)-5-bromopyridineHCID 16217843—
SolventDimethylformamideHCID 6228—
Product2-(N-BOC-N-methylamino)-5-bromopyridineHCID 1119694293.7%

Reaction Steps

Tert-butyl 5-bromopyridin-2-ylcarbamate (10 g) and cesium carbonate (20 g) were added to 50 mL of DMF. Methyl iodide (4 mL) was subsequently slowly added to the stirring reaction mixture. After 30 minutes tlc indicates that the reaction is complete. The majority of the DMF was removed under hi-vacuum and the reaction mixture was extracted with ethyl acetate and water. The organic layer was dried, filtered and concentrated. The crude product was purified by Isco 0-30% gradient (WE) over 25 mins. The tubes were pooled and concentrated to get 9.85 g of tert-butyl 5-bromopyridin-2-yl(methyl)carbamate as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158626B2
Source datasetuspto-grants-2012_04
ORD IDord-6f258aaf78414270b2971a3b76699ad4
Source noteuspto-grants-2012_04