戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 405158作成日:2026年10月25日

Tetrahydrofuran → 3-(5-(2-(((2,4'-Dichloro-2'-methyl-[1,1'-biphenyl]-4-yl)amino)methyl)-5-(trifluoromethyl)phenyl)picolinamido)propanoic acid

https://huagongshe.com/reaction/405158

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Sodium HydroxideHCID 14798—
反応物Ethyl 3-(5-(2-(((2,4'-dichloro-2'-methyl-[1,1'-biphenyl]-4-yl)amino)methyl)-5-(trifluoromethyl)phenyl)picolinamido)propanoateHCID 71060055—
溶媒MethanolHCID 887—
生成物3-(5-(2-(((2,4'-Dichloro-2'-methyl-[1,1'-biphenyl]-4-yl)amino)methyl)-5-(trifluoromethyl)phenyl)picolinamido)propanoic acidHCID 71059855—

反応手順

A 3M aqueous solution of NaOH (5.6 mL, 16.7 mmol) was added to a THF (20 mL) and MeOH (10 mL) solution of ethyl 3-(5-(2-(((2,4′-dichloro-2′-methyl-[1,1′-biphenyl]-4-yl)amino)methyl)-5-(trifluoromethyl)phenyl)picolinamido)propanoate (3.5 g, 5.6 mmol) and the resulting homogeneous mixture was stirred at room temperature. After 16 h the resulting mixture was concentrated in vacuo, suspended in water, and acidified with 2 M HCl. The resulting precipitate was filtered off, dried in vacuo, and purified via HPLC to yield the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08748624B2
出典データセットuspto-grants-2014_06
ORD IDord-bab2d4a172fe47c693bc42ae3c8777ad
出典メモuspto-grants-2014_06