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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28399생성일: 2026년 10월 25일

Potassium Carbonate → 6-{4-[4-(5-chloro-1H-indole-2-sulphonyl)-piperazine-1-carbonyl]-phenyl}-2-[2-(2-methoxy-ethoxy)-ethyl]-2H-pyridazin-3-one

https://huagongshe.com/reaction/28399

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-Bromo-3,6-dioxaheptaneHCID 123532—
반응물HCID 178519419HCID 178519419—
용매DimethylformamideHCID 6228—
생성물6-{4-[4-(5-chloro-1H-indole-2-sulphonyl)-piperazine-1-carbonyl]-phenyl}-2-[2-(2-methoxy-ethoxy)-ethyl]-2H-pyridazin-3-oneHCID 1136543236%

반응 단계

6-[4-({4-[(5-Chloro-1H-indol-2-yl)sulphonyl]piperazin-1-yl}carbonyl)phenyl]-pyridazin-3-ol (see WO 99/57113, 0.054 gram, 0.11 mmol), 0.016 gram of anhydrous potassium carbonate (0.11 mmol, 1.0 eq.) and 0.02 gram of 1-bromo-2-(2-methoxy-ethoxy)ethane (0.11 mmol, 1.0 eq.) were mixed in 1.5 mL of dry N,N-dimethylform-amide. The mixture was treated with microwave at 150° C. for 1 hour. Without any work-up, purification was performed on preparative HPLC, which gave 0.023 gram of 6-{4-[4-(5-chloro-1H-indole-2-sulphonyl)-piperazine-1-carbonyl]-phenyl}-2-[2-(2-methoxy-ethoxy)-ethyl]-2H-pyridazin-3-one (yield 36%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419979B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-8dd19348367d4871a2bcb02732782199
출처 메모uspto-grants-2008_09