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HRID 516021作成日:2026年10月24日

Triethylamine → (R)-Methyl 6-(1-amino-4-methyl-1-oxopentan-2-ylamino)-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinate

https://huagongshe.com/ja/reaction/516021

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Sodium BicarbonateHCID 516892—
反応物(R)-2-Amino-4-methylpentanamideHCID 7271815—
反応物Methyl 6-chloro-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinateHCID 58317716—
溶媒DimethylformamideHCID 6228—
生成物(R)-Methyl 6-(1-amino-4-methyl-1-oxopentan-2-ylamino)-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinateHCID 6723942050.1%

反応条件

温度60 °C

反応手順

A mixture of methyl 6-chloro-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinate (120.7 mg, 0.330 mmol), (R)-2-amino-4-methylpentanamide (67.1 mg, 0.515 mmol), and Et3N (0.1 mL, 0.717 mmol) in DMF (4 mL) was stirred at 60° C. for 14 h. Saturated aq NaHCO3 (20 mL) was added to the mixture, which was subsequently extracted with EtOAc (2×30 mL). The organic layers were washed with saturated aq NaHCO3 (20 mL), water (20 mL) and brine (20 mL), were dried over anhydrous Na2SO4, and filtered (DM1020). The filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (SiO2, hexanes/EtOAc=1/2) and then triturated with IPE to give the title compound (76 mg, 50%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09108970B2
出典データセットuspto-grants-2015_08
ORD IDord-34132de5c7ab469aa455ab8889860309
出典メモuspto-grants-2015_08