戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2113793作成日:2026年10月25日

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

反応式

関与物質

役割名称HCID仕込み量
反応物4-HeptanoneHCID 31246—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物7-(2-chloro-4,6-dimethylphenyl)-2-methyl-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-b]pyridin-3-ylamineHCID 22136278—
溶媒1,1-DichloroethaneHCID 6365—
生成物[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—

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07432283B2
出典データセットuspto-grants-2008_10
ORD IDord-b2d9520e622d4452b03569f78341784b
出典メモuspto-grants-2008_10