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HRID 1017577作成日:2026年10月25日

2,2-Dimethyl-1,3-dioxan-5-one → 3-(1-methylindol-3-yl)-4-[3-(2,2-dimethyl-1,3-dioxan-5-ylamino)phenyl]-1H-pyrrole-2,5-dione

https://huagongshe.com/reaction/1017577

反応式

関与物質

役割名称HCID仕込み量
反応物2,2-Dimethyl-1,3-dioxan-5-oneHCID 2733141—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Iron oxide, spentHCID 5327711—
溶媒MethanolHCID 887—
生成物3-(1-methylindol-3-yl)-4-[3-(2,2-dimethyl-1,3-dioxan-5-ylamino)phenyl]-1H-pyrrole-2,5-dioneHCID 1201816768.1%

反応手順

A mixture of 3-(1-methylindol-3-yl)-4-(3-aminophenyl)-1H-pyrrole-2,5-dione (200 mg, 0.63 mmol) and 2,2-dimethyl-1,3-dioxane-5-one (98 mg, 0.76 mmol) in MeOH (10 mL) was stirred at room temperature for 15 min., and then NaCNBH3 (79 mg, 1.26 mmol) was added. After stirring the reaction mixture overnight the volatiles were removed under vacuo and the residue was purified by preparatory TLC (1% MeOH/CH2Cl2) to give 3-(1-methylindol-3-yl)-4-[3-(2,2-dimethyl-1,3-dioxan-5-ylamino)phenyl]-1H-pyrrole-2,5-dione (185 mg, 68%). MS(EI): M+ 431, MP: 201-203° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06479490B2
出典データセットuspto-grants-2002_11
ORD IDord-9b2e8560d3e44f178d286171522b73fa
出典メモuspto-grants-2002_11