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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1097063생성일: 2026년 10월 26일

5-[(R)-2-{Benzyl-[2-(4-nitrophenyl)ethyl]amino}-1-(tert-butyldimethylsilanyloxy)ethyl]-8-benzyloxy-1H-quinolin-2-one → 5-[(R)-2-{[2-(4-Aminophenyl)ethyl]benzylamino}-1-(tert-butyldimethylsilanyloxy)ethyl]-8-benzyloxy-1H-quinolin-2-one

https://huagongshe.com/reaction/1097063

반응식

참여 물질

역할이름HCID투입량
반응물5-[(R)-2-{Benzyl-[2-(4-nitrophenyl)ethyl]amino}-1-(tert-butyldimethylsilanyloxy)ethyl]-8-benzyloxy-1H-quinolin-2-oneHCID 66771816—
촉매IronHCID 23925—
촉매Ferrous chloride tetrahydrateHCID 16211588—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
생성물5-[(R)-2-{[2-(4-Aminophenyl)ethyl]benzylamino}-1-(tert-butyldimethylsilanyloxy)ethyl]-8-benzyloxy-1H-quinolin-2-oneHCID 66772089—

반응 단계

A mixture of 5-[(R)-2-{benzyl-[2-(4-nitrophenyl)ethyl]amino}-1-(tert-butyldimethylsilanyloxy)ethyl]-8-benzyloxy-1H-quinolin-2-one (3.00 g, 4.52 mmol); iron (2.52 g, 45.2 mmol) and iron(II) chloride tetrahydrate (0.18 g, 0.90 mmol) in EtOH (27.3 mL) and AcOH (9.09 mL) was stirred at 80° C. overnight. The reaction mixture was filtered through a pad of Celite, washing with EtOAc (20 mL). The organic layer was washed with brine (10 mL), dried over sodium sulfate, filtered and concentrated under reduced pressure to give the title compound, which was used without any further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08138345B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-c28ecb77b33a49379c38f8a2d8b725a3
출처 메모uspto-grants-2012_03