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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 881129생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/881129

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 번호US08993600B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-ce353bf459394d0491bb9dfe0f139411
출처 메모uspto-grants-2015_03