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HRID 1017576作成日:2026年10月25日

Tetrahydro-4H-pyran-4-one → 3-(1-methylindol-3-yl)-4-(3-tetrahydropyran-4-ylaminophenyl)-1H-pyrrole-2,5-dione

https://huagongshe.com/reaction/1017576

反応式

関与物質

役割名称HCID仕込み量
反応物Tetrahydro-4H-pyran-4-oneHCID 121599—
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-tetrahydropyran-4-ylaminophenyl)-1H-pyrrole-2,5-dioneHCID 1201813970%

反応手順

A mixture of 3-(1-methylindol-3-yl)-4-(3-aminophenyl)-1H-pyrrole-2,5-dione (100 mg, 0.32 mmol) and tetrahydro-4H-pyran-4-one (65 mg, 0.65 mmol) in MeOH (8 mL) was stirred at room temperature for 40 min., and then NaCNBH3 (63 mg, 1.0 mmol) was added. After stirring the reaction mixture overnight the volatiles were removed under vacuo and the residue was purified by preparatory TLC (3% MeOH/CH2Cl2) to give 3-(1-methylindol-3-yl)-4-(3-tetrahydropyran-4-ylaminophenyl)-1H-pyrrole-2,5-dione (88.2 mg, 70%). LC/MS: M+ 401(98.6%).

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-8fa03dfec6434a34aedf7cc9e3667cee
出典メモuspto-grants-2002_11