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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21000생성일: 2026년 10월 25일

Acetic Acid → 3-Amino-6-{1-(tert-butoxycarbonyl)-5-[4-(2-hydroxyethyl)piperazin-1-ylmethyl]indol-2-yl}phthalimide

https://huagongshe.com/reaction/21000

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1-(2-Hydroxyethyl)piperazineHCID 7677—
반응물Sodium CarbonateHCID 10340—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물3-Amino-6-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]phthalimideHCID 86628226—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물3-Amino-6-{1-(tert-butoxycarbonyl)-5-[4-(2-hydroxyethyl)piperazin-1-ylmethyl]indol-2-yl}phthalimideHCID 6849203738.5%

반응 단계

3-Amino-6-[1-(tert-butoxycarbonyl)-5-formylindol-2-yl]phthalimide (45.0 mg, 0.111 mmol) was dissolved in acetonitrile (2 mL), and the solution was added with 1-(2-hydroxyethyl)piperazine (57 mg, 0.440 mmol), acetic acid (0.508 mL, 8.87 mmol) and sodium triacetoxyborohydride (118 mg, 0.557 mmol), followed by stirring at room temperature for 2.5 hours. The reaction mixture was added with water and sodium carbonate, extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by flash column chromatography (hexane/ethyl acetate=4/1, 1/1) to obtain 3-amino-6-{1-(tert-butoxycarbonyl)-5-[4-(2-hydroxyethyl)piperazin-1-ylmethyl]indol-2-yl}phthalimide (22.2 mg, yield 38%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-0a946f786c784e549ef91a1a15cd543b
출처 메모uspto-grants-2010_06