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HRID 323168作成日:2026年10月27日

Sodium borohydride → 4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(6-methoxycarbonylhexyloxy)phenyl]benzamide

https://huagongshe.com/reaction/323168

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(6-methoxycarbonyl-5-hexenyloxy)phenyl]benzamideHCID 70070581—
触媒Dichloronickel;hexahydrateHCID 11791229—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(6-methoxycarbonylhexyloxy)phenyl]benzamideHCID 2201067894.1%

反応条件

温度0 °C

反応手順

A solution of 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(6-methoxycarbonyl-5-hexenyloxy)phenyl]benzamide (360 mg) and nickel chloride hexahydrate (594 mg) in methanol (15 ml) and tetrahydrofuran (15 ml) was treated at 0° C. with sodium borohydride (283 mg) and stirred at 0° C. for 4 hours. The reaction mixture was diluted with tetrahydrofuran and filtered through a bed of Celite and then concentrated. The residue was diluted with ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate, concentrated to give 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(6-methoxycarbonylhexyloxy)phenyl]benzamide (340 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211242B1
出典データセットuspto-grants-2001_04
ORD IDord-b3afac3601d14e4897952eb973a83c22
出典メモuspto-grants-2001_04