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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15287생성일: 2026년 10월 23일

Acetic Acid → 2-(S)-(4-Fluoro-phenyl)-N-{1-(S)-[(6-methoxy-pyridin-3-ylamino)-methyl]-2-methyl-propyl}-4-morpholin-4-yl-4-oxo-butyramide

https://huagongshe.com/ko/reaction/15287

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물6-Methoxy-3-pyridinylamineHCID 81121—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물2-(S)-(4-Fluoro-phenyl)-N-(1-(S)-formyl-2-methyl-propyl)-4-morpholin-4-yl-4-oxo-butyramideHCID 86598197—
용매MethanolHCID 887—
생성물2-(S)-(4-Fluoro-phenyl)-N-{1-(S)-[(6-methoxy-pyridin-3-ylamino)-methyl]-2-methyl-propyl}-4-morpholin-4-yl-4-oxo-butyramideHCID 11363455—

반응 단계

2-(S)-(4-Fluoro-phenyl)-N-(1-(S)-formyl-2-methyl-propyl)-4-morpholin-4-yl-4-oxo-butyramide (350 mg, 0.96 mmol, 1.0 eq.) and 5-Amino-2-methoxy-pyridine (240 μL, 1.92 mmol, 2.0 eq.) dissolved in MeOH (2.5 mL) and acetic acid (106 mL, 1.92 mmol, 2.0 eq.) added via syringe at room temperature. Sodium cyanoborohydride (121 mg, 1.92 mmol, 2.0 eq.) added in portion and the reaction monitored the reaction by LC/MS. Upon completion, solvents were evaporated and dissolved in EtOAc (100 mL) washed with brine, dried over MgSO4, filtered and evaporated. Purification by preparative mass-directed HPLC provided the title compound as a white solid after evaporation and lyophilization (2.6 mg, 5.6 □mol, 0.6%). HPLC-MS calcd. for C25H33FN4O4 (M+H+) 473.3, found 473.5.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732449B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6c62c4332ef44f8489b306f4c2675391
출처 메모uspto-grants-2010_06