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HRID 56788作成日:2026年10月26日

Methyl 4-aminobenzoate → Methyl ({2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-[tetrahydro-2H-pyran-2-yl]propanoyl}amino)benzoate

https://huagongshe.com/reaction/56788

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DiisopropylcarbodiimideHCID 12734—
反応物2-[4-(5-Chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-[tetrahydro-2H-pyran-2-yl]propanoic acidHCID 117622681—
溶媒DimethylformamideHCID 6228—
生成物Methyl ({2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-[tetrahydro-2H-pyran-2-yl]propanoyl}amino)benzoateHCID 131736942—

反応手順

2.20 g (5.28 mmol) of 2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-[tetrahydro-2H-pyran-2-yl]propanoic acid (mixture of racemic diastereomers), 798 mg (5.28 mmol) of methyl 4-aminobenzoate, 750 mg (5.28 mmol) of Oxima and 822 μl (5.28 mmol) of DIC in 110 ml of dimethylformamide were reacted according to General Method 5B. The reaction mixture was purified by flash chromatography (80 g cartridge, 60 ml/min, cyclohexane/ethyl acetate gradient). Yield: 905 mg (31% 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-dbbe3062c8614077a69660130c1968ac
出典メモuspto-grants-2016_09