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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1847545생성일: 2026년 10월 27일

4-Oxobutanoic acid → 4-(5-(1-(Benzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-2-tert-butylindolin-1-yl)butanoic acid

https://huagongshe.com/reaction/1847545

반응식

참여 물질

역할이름HCID투입량
반응물4-Oxobutanoic acidHCID 1112—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물1-(Benzo[d][1,3]dioxol-5-yl)-N-(2-tert-butylindolin-5-yl)cyclopropanecarboxamideHCID 59129238—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물4-(5-(1-(Benzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-2-tert-butylindolin-1-yl)butanoic acidHCID 5912948130.1%

반응 단계

To a solution of 1-(benzo[d][1,3]dioxol-5-yl)-N-(2-tert-butylindolin-5-yl)cyclopropanecarboxamide (350 mg, 0.93 mmol, 1 eq) in anhydrous methanol (6.5 mL) and AcOH (65 μL) was added 4-oxobutanoic acid (15% in water, 710 mg, 1.0 mmol) at room temperature. After 20 min of stirring, NaBH3CN (130 mg, 2.0 mmol) was added in one portion and the reaction mixture was stirred for another 4 h at room temperature. The reaction mixture was quenched by addition of AcOH (0.5 mL) at 0° C. and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (5-75% ethyl acetate/hexanes) to give 4-(5-(1-(benzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-2-tert-butylindolin-1-yl)butanoic acid (130 mg, 30%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08952050B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-f35be9eac85f4f79a3893453fa1ca902
출처 메모uspto-grants-2015_02