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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1017646생성일: 2026년 10월 25일

Methanol → N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-4-(4-fluorophenoxy)benzamide

https://huagongshe.com/reaction/1017646

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Diphenyl chlorophosphateHCID 75654—
반응물(3R)-1-Azabicyclo(2.2.2)octan-3-amineHCID 719215—
반응물4-(4-Fluorophenoxy)benzoic acidHCID 5005163—
용매DichloromethaneHCID 6344—
생성물N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-4-(4-fluorophenoxy)benzamideHCID 992404485.2%

반응 단계

TEA (50 μL, 0.35 mmol) is added to a suspension of the acid from Step F (81 mg, 0.35 mmol) in CH2Cl2 (1 mL). Diphenylchlorophosphate (62 μL, 0.3 mmol) is added and the resulting solution is stirred at room temperature for 30 minutes. A solution of (R)-3-aminoquinuclidine (1.0M in CH3CN, 0.2 mL, 0.2 mmol) is added and the resulting solution is shaken overnight at room temperature. MeOH is added and the mixture is poured through a column of AG50W×2 ion exchange resin (H+ form). The resin is washed with MeOH and then the product is eluted with 5% TEA in MeOH. The eluent is evaporated to dryness to yield the desired product (58 mg, 85%). MS for C20H21FN2O2 (ESI) (M+H)+ m/z 341.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06479510B2
출처 데이터셋uspto-grants-2002_11
ORD IDord-7083cc2633834f7ba5f83c5c9cf1f6a5
출처 메모uspto-grants-2002_11