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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1783875생성일: 2026년 10월 25일

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/reaction/1783875

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 번호US07501408B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-950430614803451d89e67ca6730e7c21
출처 메모uspto-grants-2009_03