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HRID 56665作成日:2026年10月26日

Methyl 4-aminobenzoate → Methyl 4-[(2-{4-[5-chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-cyclopropylpropanoyl)amino]benzoate

https://huagongshe.com/reaction/56665

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-aminobenzoateHCID 12082—
反応物2-{4-[5-Chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-cyclopropylpropanoic acidHCID 117622693—
生成物Methyl 4-[(2-{4-[5-chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-cyclopropylpropanoyl)amino]benzoateHCID 117622871—

反応手順

105 mg (purity 94%, 0.26 mmol) of 2-{4-[5-chloro-2-(trifluoromethyl)phenyl]-2-oxopyridin-1(2H)-yl}-3-cyclopropylpropanoic acid (racemate) and 1.1 eq. of methyl 4-aminobenzoate were reacted according to General Method 5A. After aqueous work-up, the crude product was reacted further without further purification. Yield: 200 mg (purity 48%, 72% of theory)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434690B2
出典データセットuspto-grants-2016_09
ORD IDord-1b998f1cadf143c191a279708de4e710
出典メモuspto-grants-2016_09