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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 453686생성일: 2026년 10월 25일

3-(2-Bromoacetyl)benzonitrile → (R)-1-(2-(3-cyanophenyl)-2-oxoethyl)-3-((R)-2-phenyl-2-(phenylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane bromide

https://huagongshe.com/reaction/453686

반응식

참여 물질

역할이름HCID투입량
반응물3-(2-Bromoacetyl)benzonitrileHCID 2735867—
반응물(R)-((R)-quinuclidin-3-yl) 2-phenyl-2-(phenylamino)acetateHCID 46840261—
용매Ethyl AcetateHCID 8857—
생성물(R)-1-(2-(3-cyanophenyl)-2-oxoethyl)-3-((R)-2-phenyl-2-(phenylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane bromideHCID 8666030061%

반응 단계

3-(2-Bromoacetyl)benzonitrile (40.0 mg, 0.18 mmol) was added to a solution of (R)—((R)-quinuclidin-3-yl) 2-phenyl-2-(phenylamino)acetate (diastereomer 1 of I2) (60 mg, 0.18 mmol) in EtOAc (2 ml). The reaction mixture was stirred at room temperature overnight (UPLC-MS: complete conversion). EtOAc was removed under vacuum, and the residue is triturated with Et2O. The solid was collected by suction filtration and dried at 40° C. for 48 hours to obtain the (R)-1-(2-(3-cyanophenyl)-2-oxoethyl)-3-((R)-2-phenyl-2-(phenylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane bromide (61.1 mg, 61% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492548B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-19944274fdfb450c86b7b3ae2a8d921c
출처 메모uspto-grants-2013_07