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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77404생성일: 2026년 10월 24일

1,4-Diazabicyclo(3.2.2)nonane → 7-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-one

https://huagongshe.com/ko/reaction/77404

반응식

참여 물질

역할이름HCID투입량
반응물1,4-Diazabicyclo(3.2.2)nonaneHCID 398407—
반응물Binap, (A+-)-HCID 634876—
반응물Sodium t-butoxideHCID 23676156—
반응물7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-oneHCID 69928548—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물7-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-oneHCID 5135344435%

반응 조건

온도85 °C

반응 단계

A mixture of 7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-one (Intermediate 24A) (50 mg, 0.143 mmol), 1,4-diazabicyclo[3.2.2]nonane (27.2 mg, 0.215 mmol), sodium t-butoxide (55.1 mg, 0.574 mmol), tris(dibenzylideneacetone)dipalladium(0) (13.13 mg, 0.014 mmol) and (+/−) BINAP (26.8 mg, 0.043 mmol) in degassed dioxane (1 mL) was heated to 85° C. under N2 in a sealed vessel overnight. Reaction mixture allowed to cool to room temperature, diluted with water and the product extracted into ethyl acetate. Organics washed several times with water, dried (MgSO4), filtered and then evaporated to dryness. The crude product was added to a silica gel column (25 g) and was eluted with 0-50% 2M ammonia in methanol in ethylacetate to afford 7-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-3-(3-chlorophenyl)-2-methylisoquinolin-1(2H)-one (19.4 mg, 0.05 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841289B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-c1d1c04561374a87909533458de57e09
출처 메모uspto-grants-2014_09