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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 562013생성일: 2026년 10월 25일

1,1-dimethylethyl 4-[7-(aminocarbonyl)-5-bromo-1H-indol-3-yl]-3,6-dihydro-1(2H)-pyridinecarboxylate → tert-butyl 4-(5-bromo-7-carbamoyl-1H-indol-3-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/562013

반응식

참여 물질

역할이름HCID투입량
반응물1,1-dimethylethyl 4-[7-(aminocarbonyl)-5-bromo-1H-indol-3-yl]-3,6-dihydro-1(2H)-pyridinecarboxylateHCID 59600656—
촉매Platinum oxide (PtO)HCID 82844—
용매EthanolHCID 702—
생성물tert-butyl 4-(5-bromo-7-carbamoyl-1H-indol-3-yl)piperidine-1-carboxylateHCID 5960066048.3%

반응 단계

To a solution of 1,1-dimethylethyl 4-[7-(aminocarbonyl)-5-bromo-1H-indol-3-yl]-3,6-dihydro-1(2H)-pyridinecarboxylate (7.41 g, 17.64 mmol) in ethanol (600 mL), platinum oxide (200 mg, 5%) was added. The reaction mixture was hydrogenated under an atmosphere of H2 for 16 hours. The resulting mixture was filtered through celite and the filtrate was concentrated. The resulting residue was purified by flash column chromatography (Ethyl acetate/hexanes, 1:4 to 2:1 v/v) to give the desired product (3.6 g, 48%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063071B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-5e3c8c72eef24a21aaa49d1c7556cc62
출처 메모uspto-grants-2011_11