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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 573655생성일: 2026년 10월 26일

Potassium Carbonate → 3-Chloro-N-[2-(4-isoquinolinyl)-3,6-dimethylthieno[2,3-b]pyridin-4-yl]benzenesulfonamide

https://huagongshe.com/reaction/573655

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Isoquinoline-4-boronic acidHCID 3761204—
반응물N-(2-bromo-3,6-dimethylthieno[2,3-b]pyridin-4-yl)-3-chlorobenzenesulfonamideHCID 68324042—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물3-Chloro-N-[2-(4-isoquinolinyl)-3,6-dimethylthieno[2,3-b]pyridin-4-yl]benzenesulfonamideHCID 6832390737.2%

반응 조건

온도100 °C

반응 단계

To a solution of N-(2-bromo-3,6-dimethylthieno[2,3-b]pyridin-4-yl)-3-chlorobenzenesulfonamide (Example 77) (100 mg, 0.232 mmol) in 1,4-dioxane (2 mL) and water (1 mL) was added 4-isoquinolinylboronic acid (40.1 mg, 0.232 mmol), bis(triphenylphosphine)palladium(II) chloride (16.26 mg, 0.023 mmol) and potassium carbonate (112 mg, 0.811 mmol) and the mixture heated at 100° C. for 1 h using a microwave reactor. The mixture was then filtered through celite, washing with ethyl acetate (30 mL) and the filtrate evaporated to dryness. The residue was then purified by MDAP (acidic conditions), to afford the title compound (41.45 mg). LCMS (A) m/z: 480 [M+1]+, Rt 1.13 min (acidic).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029545B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-df96f4948d40466e8266fbf0709b341c
출처 메모uspto-grants-2015_05