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HRID 1388931作成日:2026年10月27日

Ethyl 4-methoxy-3-ethoxycarbonyl-1-methylpyrrole-2-acetate → [4-Methoxy-1-methyl-5-(2-methylbenzoyl)-1H-pyrrol-2-yl]acetic acid

https://huagongshe.com/reaction/1388931

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 4-methoxy-3-ethoxycarbonyl-1-methylpyrrole-2-acetateHCID 20469092—
反応物5-(o-Methylbenzoyl)-4-methoxy-3-ethoxycarbonyl-1-methylpyrrole-2-acetateHCID 20469113—
反応物5-(o-Methylbenzoyl)-4-methoxy-3-hydroxycarbonyl-1-methylpyrrole-2-acetic acidHCID 20469154—
溶媒Trifluoroacetic acidHCID 6422—
生成物[4-Methoxy-1-methyl-5-(2-methylbenzoyl)-1H-pyrrol-2-yl]acetic acidHCID 2046908950%

反応手順

Following substantially the procedures as described in Example 1, Steps C-E, crude ethyl 4-methoxy-3-ethoxycarbonyl-1-methylpyrrole-2-acetate is converted to about 16 mmole of 5-(o-methylbenzoyl)-4-methoxy-3-ethoxycarbonyl-1-methylpyrrole-2-acetate followed by hydrolysis to 5-(o-methylbenzoyl)-4-methoxy-3-hydroxycarbonyl-1-methylpyrrole-2-acetic acid which in turn is decarboxylated in neat TFA according to procedure of Example 2 to afford an overall 50% yield of 5-(o-methylbenzoyl)-4-methoxy-1-methylpyrrole-2-acetic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04434175
出典データセットuspto-grants-1984_02
ORD IDord-96574269ed3d4b2091a51409e088389a
出典メモuspto-grants-1984_02