戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2297535作成日:2026年10月25日

1-(1,3-benzodioxol-5-yl)-2,3,4,9-tetrahydro-1H-beta-carboline → 1-Benzo[1,3]dioxol-5-yl-2-[5-(3,4-dimethoxy-phenyl)-pyrimidin-2-yl]-2,3,4,9-tetrahydro-1H-beta-carboline

https://huagongshe.com/reaction/2297535

反応式

関与物質

役割名称HCID仕込み量
反応物1-(1,3-benzodioxol-5-yl)-2,3,4,9-tetrahydro-1H-beta-carbolineHCID 201172—
反応物2-Chloro-5-(3,4-dimethoxyphenyl)pyrimidineHCID 3486989—
溶媒DimethylformamideHCID 6228—
生成物1-Benzo[1,3]dioxol-5-yl-2-[5-(3,4-dimethoxy-phenyl)-pyrimidin-2-yl]-2,3,4,9-tetrahydro-1H-beta-carbolineHCID 11049430—

反応条件

温度120 °C

反応手順

A solution of 1-(3,4-methylenedioxyphenyl)-2,3,4,9-tetrahydro-1H-β-carboline (3.73 g, 12.8 mmol) (prepared according to the process as disclosed in WO97/43287, Intermediate 7, page 24) and 2-chloro-5-(3,4-dimethoxyphenyl)pyrimidine (1.6 g, 6.4 mmol) in DMF (50 mL, anhydrous) was heated at 120° C. under stirring for 16 h. The reaction mixture was quenched with NH4Cl and extracted with ethyl acetate. The organic phase was washed with brine (2×) and dried with MgSO4. Column chromatography (silica gel, ethyl acetate:hexanes=2:3) yielded a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06492358B2
出典データセットuspto-grants-2002_12
ORD IDord-b57604f585684046889db62e0b3989d7
出典メモuspto-grants-2002_12