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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1512009생성일: 2026년 10월 26일

L-Alanine → 2-(S)-{[4-(4-Fluoro-benzyl)-1-hydroxy-3-oxo-6-trifluoromethyl-3,4-dihydro-4,4a-diaza-fluorene-2-carbonyl]-amino}-propionic acid

https://huagongshe.com/reaction/1512009

반응식

참여 물질

역할이름HCID투입량
반응물L-AlanineHCID 5950—
반응물Sodium MethoxideHCID 10942334—
반응물4-(4-Fluoro-benzyl)-1-hydroxy-3-oxo-6-trifluoromethyl-3,4-dihydro-4,4a-diaza-fluorene-2-carboxylic acid methyl esterHCID 68762405—
용매2-MethoxyethanolHCID 8019—
생성물2-(S)-{[4-(4-Fluoro-benzyl)-1-hydroxy-3-oxo-6-trifluoromethyl-3,4-dihydro-4,4a-diaza-fluorene-2-carbonyl]-amino}-propionic acidHCID 5475117430.1%

반응 단계

A mixture of 4-(4-fluoro-benzyl)-1-hydroxy-3-oxo-6-trifluoromethyl-3,4-dihydro-4,4a-diaza-fluorene-2-carboxylic acid methyl ester (compound 43 d) (100 mg, 0.23 mmol), L-alanine (205 mg, 2.3 mmol) and sodium methoxide (99 mg, 1.84 mmol) in 2-methoxyethanol (3.5 mL) was microwaved at 150° C. for 2 h and concentrated. Residue was dissolved in water (80 mL), acidified to pH=3-4 using 1 N HCl solution and extracted with EtOAc. Organic layer was washed with brine, dried over MgSO4, filtered and concentrated. Crude product was purified by silica gel chromatography (15%-70% EtOAc (with 0.075% HOAc)/hexanes (with 0.1% HOAc)) to provide the title compound 34 mg. ESI (m/z): 490.03 (M−H)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08217043B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-5a68a2a83e324bd8aa7f1d6fa10981e7
출처 메모uspto-grants-2012_07