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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22999생성일: 2026년 10월 26일

Hydrochloric Acid → 3-(5-chloro-1-methyl-1H-indol-3-yl)-4-[1-[3-[(methylsulfonyl)oxy]propyl]-1H-indazol-3-yl]-1H-pyrrole-2,5-dione

https://huagongshe.com/reaction/22999

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PyridineHCID 1049—
반응물Methanesulfonic anhydrideHCID 81560—
반응물3-(5-chloro-1-methyl-1H-indol-3-yl)-4-[1-(3-hydroxypropyl)-1H-indazol-3-yl]-1H-pyrrole-2,5-dioneHCID 10224909—
용매TetrahydrofuranHCID 8028—
생성물3-(5-chloro-1-methyl-1H-indol-3-yl)-4-[1-[3-[(methylsulfonyl)oxy]propyl]-1H-indazol-3-yl]-1H-pyrrole-2,5-dioneHCID 22591932—

반응 조건

온도50 °C

반응 단계

Pyridine (0.37 g, 4.62 mmol) and methanesulfonic anhydride (0.54 g, 3.08 mmol) were added to Compound 74 (0.67 g, 1.54 mmol) in THF (10 mL). The mixture was heated at 50° C. for 2 h, then cooled to rt. Another portion of THF (5 mL) was added, Followed by 1N HCl (5 mL). The mixture was stirred for another 15 min, then extracted with EtOAc, several times. The combined EtOAc layers were washed once with 1N HCl (10 mL), water (2×20 mL) and saturated NaCl (20 mL), then dried (Na2SO4) and evaporated in vacuo to obtain 3-(5-chloro-1-methyl-1H-indol-3-yl)-4-[1-[3-[(methylsulfonyl)oxy]propyl]-1H-indazol-3-yl]-1H-pyrrole-2,5-dione as Compound 26a (0.73 g, 92%) as a reddish solid. ES-MS m/z 513 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849643B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-560ee865923648af9f817541c30ea563
출처 메모uspto-grants-2005_02