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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 453691생성일: 2026년 10월 26일

2-Bromo-2'-acetonaphthone → (R)-1-(2-(naphthalen-2-yl)-2-oxoethyl)-3-((R)-2-phenyl-2-(phenylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane bromide

https://huagongshe.com/reaction/453691

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-2'-acetonaphthoneHCID 69179—
반응물(R)-((R)-quinuclidin-3-yl) 2-phenyl-2-(phenylamino)acetateHCID 46840261—
용매AcetonitrileHCID 6342—
생성물(R)-1-(2-(naphthalen-2-yl)-2-oxoethyl)-3-((R)-2-phenyl-2-(phenylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane bromideHCID 5477130894.6%

반응 조건

온도100 °C

반응 단계

To a solution of (R)—((R)-quinuclidin-3-yl) 2-phenyl-2-(phenylamino)acetate (diastereomer 1 of I2) (75 mg, 0.22 mmol) in acetonitrile (5 ml), was added 2-bromo-1-(naphthalen-2-yl)ethanone (55.5 mg, 0.22 mmol) and the reaction was stirred at 100° C. for 70 minutes under microwave irradiation (UPLC-MS: complete conversion). The solvent was evaporated and the crude was triturated with i-Pr2O-EtOAc (9/1) to obtain (R)-1-(2-(naphthalen-2-yl)-2-oxoethyl)-3-((R)-2-phenyl-2-(phenylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane bromide (121.9 mg, 93% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492548B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-76c6a67004fc4d24ac3ab0742093a29d
출처 메모uspto-grants-2013_07