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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2113793생성일: 2026년 10월 26일

4-Heptanone → [7-(2-chloro-4,6-dimethylphenyl)-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridin-3-yl](1-propylbutyl)amine

https://huagongshe.com/reaction/2113793

반응식

참여 물질

역할이름HCID투입량
반응물4-HeptanoneHCID 31246—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물7-(2-chloro-4,6-dimethylphenyl)-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridin-3-ylamineHCID 22136278—
용매1,1-DichloroethaneHCID 6365—
생성물[7-(2-chloro-4,6-dimethylphenyl)-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridin-3-yl](1-propylbutyl)amineHCID 22136272—

반응 조건

온도60 °C

반응 단계

7-(2-Chloro-4,6-dimethylphenyl)-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridin-3-ylamine (5-45; 45.7 mg) and 4-heptanone (24 μL) were dissolved and stirred in 3 mL of dichloroethane. After 15 min, 44.5 mg of sodium triacetoxyborohydride was added. The reaction mixture was stirred at 60° C. during the day and at room temperature over night during 3 d. During this period, an additional 109 μL of 4-heptanone and an additional 104 mg of sodium triacetoxyborohydride were added to drive the reaction to completion. The reaction mixture was then partitioned between ethyl acetate and water. The ethyl acetate was dried with magnesium sulfate and evaporated. The crude product was chromatographed on silica gel eluting with an acetone/hexane gradient to provide 11 mg of crystalline [7-(2-chloro-4,6-dimethylphenyl)-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridin-3-yl](1-propylbutyl)amine (5-6): ms (MH+)=389.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07432283B2
출처 데이터셋uspto-grants-2008_10
ORD IDord-b2d9520e622d4452b03569f78341784b
출처 메모uspto-grants-2008_10