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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21335생성일: 2026년 10월 24일

Acetic Acid → 4-methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-5-[N-(2-methoxyethyl)methylaminomethyl]indol-2-yl]isoindolinone

https://huagongshe.com/ko/reaction/21335

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물(2-Methoxyethyl)(methyl)amineHCID 300977—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물4-Methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinoneHCID 86628301—
용매AcetonitrileHCID 6342—
생성물4-methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-5-[N-(2-methoxyethyl)methylaminomethyl]indol-2-yl]isoindolinoneHCID 8662833560%

반응 단계

In a similar manner to Step 2 of Example 6, 4-methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]isoindolinone (856 mg, 1.71 mmol) was dissolved in acetonitrile (17.0 mL), and the solution was treated with (2-methoxyethyl)methylamine (2.76 mL, 25.7 mmol), acetic acid (1.47 mL, 25.7 mmol) and sodium triacetoxyborohydride (1.81 g, 8.56 mmol), followed by purification by flash column chromatography (chloroform/methanol=4/1) to obtain 4-methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-5-[N-(2-methoxyethyl)methylaminomethyl]indol-2-yl]isoindolinone (586 mg, 60%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-052f6ee7314f49b880d98e5af242cf98
출처 메모uspto-grants-2010_06