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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21294생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/21294

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물N-MethylethylamineHCID 12219—
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-methylethylaminomethyl)indol-2-yl]isoindolinoneHCID 8662831262%

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 (100 mg, 0.200 mmol) was dissolved in acetonitrile (5.8 mL), and the solution was treated with N-methylethylamine (0.160 mL, 2.00 mmol), acetic acid (0.229 mL, 4.00 mmol) and sodium triacetoxyborohydride (211 mg, 0.996 mmol), followed by purification by preparative thin-layer chromatography (chloroform/methanol=4/1) to obtain 4-methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-5-(N-methylethylaminomethyl)indol-2-yl]isoindolinone (67.0 mg, yield 62%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ce9f1a9e0bcd4f128e0477aed01f71dd
출처 메모uspto-grants-2010_06