戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2297536作成日:2026年10月26日

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 1-(3,4-Methylenedioxy-phenyl)-2-[5-(4-methoxyphenyl)-pyrimidin-2-yl-]-4-hydoxy-2,3,4,9-tetrahydro-1H-beta-carboline

https://huagongshe.com/reaction/2297536

反応式

関与物質

役割名称HCID仕込み量
反応物2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
反応物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—
反応物Oxolane--water (1/1)HCID 21881883—
溶媒Ethyl AcetateHCID 8857—
生成物1-(3,4-Methylenedioxy-phenyl)-2-[5-(4-methoxyphenyl)-pyrimidin-2-yl-]-4-hydoxy-2,3,4,9-tetrahydro-1H-beta-carbolineHCID 12020639—

反応条件

温度0 °C

反応手順

To a mixture of DDQ (113.5 mg, 0.5 mmol) and 1-(3,4-methylenedioxyphenyl)-2-[5-(3,4-dimethoxyphenyl)pyrimidin-2-yl]-2,3,4,9-tetrahydro-1H-β-carboline (prepared as in Example 3) (51 mg, 0.1 mmol) was added a mixed solvent of THF:water (9:1) at −78° C. The mixture was stirred at 0° C. and allowed to warm to room temperature over a period of 15 h. Column chromatography (silica gel, hexanes:ethyl acetate=1:1) yielded the-oxo- and -hydroxy derivatives respectively, as white solids.

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-4f2fa12b1b6b46efaa49296db3acb482
出典メモuspto-grants-2002_12