戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 562306作成日:2026年10月25日

O-Methylhydroxylamine → 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(3-{[(methyloxy)imino]methyl}phenyl)-1H-indole-7-carboxamide

https://huagongshe.com/reaction/562306

反応式

関与物質

役割名称HCID仕込み量
反応物O-MethylhydroxylamineHCID 4113—
反応物3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(3-formylphenyl)-1H-indole-7-carboxamideHCID 57732804—
溶媒Dimethyl SulfoxideHCID 679—
生成物3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(3-{[(methyloxy)imino]methyl}phenyl)-1H-indole-7-carboxamideHCID 8663103556%

反応手順

To a solution of 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(3-formylphenyl)-1H-indole-7-carboxamide (50 mg, 0.114 mmol) in DMSO (3.0 mL) was added O-methylhydroxylamine (57 mg, 0.684 mmol). The reaction was stirred overnight. Additional O-methylhydroxylamine (0.342 mmol) was added to the reaction mixture and stirred for 48 h. The solvent was then concentrated and purified by Gilson Preparatory HPLC to give 29.8 mg of 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(3-{[(methyloxy)imino]methyl}phenyl)-1H-indole-7-carboxamide (56%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063071B2
出典データセットuspto-grants-2011_11
ORD IDord-ac143cd465f14b1db6ac31f348fb3374
出典メモuspto-grants-2011_11