돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 401579생성일: 2026년 10월 25일

Potassium Carbonate → tert-butyl 6-(4-(N-methylsulfamoyl)phenyl)pyridin-2-ylcarbamate

https://huagongshe.com/reaction/401579

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Tert-butyl (6-bromopyridin-2-YL)carbamateHCID 13040380—
반응물4-((Methylamino)sulphonyl)benzene boronic acidHCID 44118763—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물tert-butyl 6-(4-(N-methylsulfamoyl)phenyl)pyridin-2-ylcarbamateHCID 5916617772.2%

반응 조건

온도80 °C

반응 단계

To a solution of 4-(N-methylsulfamoyl)phenylboronic acid (17.2 g, 0.08 mol) and (6-bromo-pyridin-2-yl)carbamic acid tert-butyl ester (21.9 g, 0.08 mol) in DMF (125 mL) and H2O (125 mL) were added Pd(PPh3)4 (9.2 g, 0.008 mol) and K2CO3 (16.6 g, 0.12 mol). The resulting mixture was degassed by gently bubbling argon through the solution for 5 minutes at 20° C. The reaction mixture was then heated at 80° C. for 16 h. The mixture was evaporated under reduced pressure, then poured into H2O, and extracted with EtOAc. The organic phase was dried over Na2SO4, and was evaporated under reduced pressure to give tert-butyl 6-(4-(N-methylsulfamoyl)phenyl)pyridin-2-ylcarbamate (21 g, 58%), which was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741933B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-2eb8d0ce5db943a183f86d1988fe29d5
출처 메모uspto-grants-2014_06