戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 42253作成日:2026年10月25日

Dimethylformamide → 2-[6-(1H-Indol-4-yl)-1H-indazol-4-yl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/42253

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Phthalic AnhydrideHCID 6811—
反応物6-(1H-indol-4-yl)-1H-indazol-4-amineHCID 58268019—
溶媒DichloromethaneHCID 6344—
生成物2-[6-(1H-Indol-4-yl)-1H-indazol-4-yl]-1H-isoindole-1,3(2H)-dioneHCID 4454040463.1%

反応条件

温度150 °C

反応手順

A mixture of 6-(1H-indol-4-yl)-1H-indazol-4-amine (500 mg, 2.014 mmol), 2-benzofuran-1,3-dione (298 mg, 2.014 mmol) and DMF (2.5 ml) was placed in a Biotage vial (2-5 ml) equipped with a magnetic stirrer bar. The vial was placed in a Biotage Initiator microwave and heated at 150° C. for 30 min then again at 150° C. for a further 15 min. The reaction mixture was evaporated to dryness to give a brown oil which was dissolved in dichloromethane and applied to a 100 g silica SPE cartridge. The cartridge was eluted on a Flashmaster (II) instrument using a gradient of 0-100% ethyl acetate in cyclohexane over 40 min followed by 0-20% methanol in cyclohexane over 15 min. Appropriate fractions were combined and evaporated to give the title compound (481 mg) as a pale yellow foam.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536169B2
出典データセットuspto-grants-2013_09
ORD IDord-86134a09b94647c7bd01f6a44bdf76c2
出典メモuspto-grants-2013_09