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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 516021생성일: 2026년 10월 24일

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

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

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium BicarbonateHCID 516892—
반응물(R)-2-Amino-4-methylpentanamideHCID 7271815—
반응물Methyl 6-chloro-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinateHCID 58317716—
용매DimethylformamideHCID 6228—
생성물(R)-Methyl 6-(1-amino-4-methyl-1-oxopentan-2-ylamino)-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinateHCID 6723942050.1%

반응 조건

온도60 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108970B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-34132de5c7ab469aa455ab8889860309
출처 메모uspto-grants-2015_08