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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 750377생성일: 2026년 10월 27일

Sodium Hydroxide → (3S)-3-amino-2-hydroxy-N-[(1R)-1-phenylethyl]heptanamide

https://huagongshe.com/reaction/750377

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물(2S)-2-{[(benzyloxy)carbonyl]amino}-1-({[(1R)-1-phenylethyl]amino}carbonyl)hexyl benzoateHCID 11202880—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물(3S)-3-amino-2-hydroxy-N-[(1R)-1-phenylethyl]heptanamideHCID 1126556095.2%

반응 단계

A mixture of 8.75 g (17.4 mmol) of (2S)-2-{[(benzyloxy)carbonyl]amino}-1-({[(1R)-1-phenylethyl]amino}carbonyl)hexyl benzoate and 6.97 g (174 mmol) of sodium hydroxide in 175 mL of dioxane and 75 mL of water was heated at reflux for 3 h. Upon cooling to room temperature, the reaction mixture was diluted with 100 mL of water and extracted with ethyl acetate. The combined ethyl acetate layers were dried over potassium carbonate and concentrated to afford 4.38 g (95%) of (3S)-3-amino-2-hydroxy-N-[(1R)-1-phenylethyl]heptanamide as a white solid. 1H NMR (300 MHz, DMSO-d6) δ 8.08 (d, J=8 Hz, 1H), 7.39-7.20 (m, 5H), 4.99 (m, 1H), 4.51 (br s, 1H), 3.71 (d, J=3 Hz, 1H), 2.81 (m, 1H), 1.50-1.05 (m, 9H), 0.87 (t, 3H). ES-LCMS m/z 265 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07402606B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-bae9cd00dec04a909affc48fd48dcc55
출처 메모uspto-grants-2008_07