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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 572205생성일: 2026년 10월 27일

4-Methylmorpholine → 5-amino-N-(3-{(1S)-1-[(6-chloropyrazin-2-yl)amino]ethyl}phenyl)nicotinamide

https://huagongshe.com/reaction/572205

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물5-Aminonicotinic AcidHCID 354316—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물(S)-N-(1-(3-aminophenyl)ethyl)-6-chloropyrazin-2-amineHCID 25218447—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물5-amino-N-(3-{(1S)-1-[(6-chloropyrazin-2-yl)amino]ethyl}phenyl)nicotinamideHCID 5933173838%

반응 단계

To a mixture of 5-aminonicotinic acid (35 mg, 0.25 mmol), N-[(1S)-1-(3-aminophenyl)ethyl]-6-chloropyrazin-2-amine (125 mg, 0.5 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (95 mg, 0.5 mmol) in N,N-dimethylformamide (2 mL) was added 1-hydroy-7-azabenzotriazole (1 mL, 0.5-0.7M in N,N-dimethylformamide, 0.5 mmol) then N-methylmorpholine (0.055 mL, 0.5 mmol) and the mixture was stirred at room temperature for 16 hours. After this time the mixture was diluted with ethyl acetate (40 mL), washed successively with saturated aqueous sodium hydrogen carbonate (2×30 mL) and brine (30 mL), dried (Na2SO4) and concentrated under reduced pressure to give a yellow oil which was purified by flash chromatography (silica, ethyl acetate/methanol) to give 5-amino-N-(3-{(1S)-1-[(6-chloropyrazin-2-yl)amino]ethyl}phenyl)nicotinamide (35 mg, 38%) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029386B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-bb941c54a4cd44a8bf80f79806521a7f
출처 메모uspto-grants-2015_05