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HRID 31469作成日:2026年10月25日

Sodium ethoxide → 5-Fluoro-6-methyl-1,1'-biphenyl-3-carboxamide

https://huagongshe.com/reaction/31469

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ethoxideHCID 2723922—
反応物4'-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-N-cyclopropyl-5-fluoro-6-methyl-1,1'-biphenyl-3-carboxamideHCID 69314917—
溶媒EthanolHCID 702—
生成物5-Fluoro-6-methyl-1,1'-biphenyl-3-carboxamideHCID 86604697—

反応手順

Freshly prepared sodium ethoxide in ethanol (0.2M, 0.8 ml) was added to a solution of (4′-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-N-cyclopropyl-5-fluoro-6-methyl-1,1′-biphenyl-3-carboxamide (Intermediate 34) (50 mg) in ethanol (1 ml) and the reaction stirred at room temperature for 18 hours. The reaction was reduced to dryness under vacuum and the residue partitioned between ethyl acetate and water. The organic phase dried (magnesium sulphate) and reduced to dryness under vacuum. The residue was purified by HPLC to give N-cyclopropyl-4′-[5-ethoxymethyl)-1,3,4-oxadiazol-2-yl]-5-fluoro-6-methyl-1,1′-biphenyl-3-carboxamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425555B2
出典データセットuspto-grants-2008_09
ORD IDord-01140e8d3fa24085a648bb18a36c93a3
出典メモuspto-grants-2008_09