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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20982생성일: 2026년 10월 24일

Acetic Acid → tert-butyl 4-(1H-indol-5-ylamino)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/20982

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium CarbonateHCID 10340—
반응물5-AminoindoleHCID 78867—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물tert-butyl 4-(1H-indol-5-ylamino)piperidine-1-carboxylateHCID 66650318125.6%

반응 단계

5-Aminoindole (100 mg, 0.757 mmol) was dissolved in acetonitrile (2 mL), and the solution was added with 1-(tert-butoxycarbonyl)-4-piperidinone (181 mg, 0.908 mmol), acetic acid (0.870 mL, 15.2 mmol) and sodium triacetoxyborohydride (160 mg, 0.755 mmol) little by little, followed by stirring at room temperature for 1 hour. The reaction mixture was added with water and sodium carbonate to adjust the pH to 9. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated to obtain 5-[1-(tert-butoxycarbonyl)-4-piperidylamino]indole (300 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-7553ba8747dd4129bdae1918f61fc2ba
출처 메모uspto-grants-2010_06