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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1630089생성일: 2026년 10월 26일

(S)-2-amino-3-(benzyloxy)-N-(4-(4-fluorophenoxy)phenyl)propanamide → (S)-2-(3-(3,5-dimethylisoxazol-4-yl)ureido)-3-benzyloxy-N-(4-(4-fluorophenoxy)phenyl)propanamide

https://huagongshe.com/reaction/1630089

반응식

참여 물질

역할이름HCID투입량
반응물(S)-2-amino-3-(benzyloxy)-N-(4-(4-fluorophenoxy)phenyl)propanamideHCID 67009137—
반응물3,5-Dimethylisoxazol-4-ylcarbamic acid hydrochlorideHCID 67010678—
생성물(S)-2-(3-(3,5-dimethylisoxazol-4-yl)ureido)-3-benzyloxy-N-(4-(4-fluorophenoxy)phenyl)propanamideHCID 45376096—

반응 단계

Proceeding as in Example 1, but substituting (S)-2-amino-3-(benzyloxy)-N-(4-(4-fluorophenoxy)phenyl)propanamide and 3,5-dimethylisoxazol-4-ylcarbamic acid hydrochloride, gave Compound 172, (S)-2-(3-(3,5-dimethylisoxazol-4-yl)ureido)-3-benzyloxy-N-(4-(4-fluorophenoxy)phenyl)propanamide. Major isomer: 1H-NMR (400 MHz, DMSO-D6): σ 11.99 (br s, 1H), 9.62 (br s, 1H), 8.40-8.38 (d, 1H), 7.55 (s, 1H), 7.36-7.19 (m, 8H), 7.07-7.02 (m, 2H), 6.94-6.76 (m, 3H), 4.74-4.69 (m, 1H), 4.53 (s, 2H), 3.77-3.64 (m, 2H), 3.53-3.42 (m, 2H), 2.06 (s, 3H). MS (EI) for C28H27FN4O4. found 503.0 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08791102B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-70415716c22d43a2ac81990b4f3ab805
출처 메모uspto-grants-2014_07