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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (R)-2-Amino-4-methylpentanamide | HCID 7271815 | — |
| 반응물 | Methyl 6-chloro-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinate | HCID 58317716 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (R)-Methyl 6-(1-amino-4-methyl-1-oxopentan-2-ylamino)-4-cyano-2-(3-(methylsulfonyl)phenylamino)nicotinate | HCID 67239420 | 50.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09108970B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-34132de5c7ab469aa455ab8889860309 |
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| 출처 메모 | uspto-grants-2015_08 |
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