Methyl chloroformate → HCID 57924514, compound

To a solution of compound 3-bromopyridin-4-amine (3 g, 17.4 mmol.) in 20 mL of anhydrous THF was added a solution of LiHMDS (1M in THF, 36.4 mL, 36.4 mmol) at 0° C. After stirring for 30 min, methyl chloroformate (2 g, 20.8 mmol) was added at 0° C. The reaction mixture was stirred at 0° C. for 2 hrs and then at r.t. overnight. The reaction was quenched with saturated aqueous ammonium chloride. The organic solvent was evaporated and the aqueous layer was extracted with ethyl acetate. The organic layers were dried over Na2SO4, concentrated. The crude product was purified by silica gel column chromatography (Petroleum ether:Ethyl acetate=1:2) to afford methyl 3-bromopyridin-4-ylcarbamate (2.34 g, 59%).

1. stirringThe reaction mixture was stirred at 0° C. for 2 hrs
2. customat r.t.
3. customovernight
4. customThe reaction was quenched with saturated aqueous ammonium chloride
5. customThe organic solvent was evaporated
6. extractionthe aqueous layer was extracted with ethyl acetate
7. dry with materialThe organic layers were dried over Na2SO4
8. concentrationconcentrated
9. customThe crude product was purified by silica gel column chromatography (Petroleum ether:Ethyl acetate=1:2)

ORD record

ord-90da5523b55f4c6ab3bf47648a9bd694

Source dataset

uspto-grants-2011_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08048862B2