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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1433782생성일: 2026년 10월 27일

(R)-1,2-Epoxypropane → (R)-tert-Butoxycarbonylamino-[4-((R)-2-hydroxy-propoxy)-phenyl]-acetic acid

https://huagongshe.com/reaction/1433782

반응식

참여 물질

역할이름HCID투입량
반응물(R)-1,2-EpoxypropaneHCID 146261—
반응물(2S,3R)-3-(benzyloxy)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)butanoic acidHCID 16213170—
반응물(R)-tert-butoxycarbonylamino-{4-[2-(tetrahydropyran-2-yloxy)-ethoxy]-phenyl}-acetic acidHCID 68617730—
생성물(R)-tert-Butoxycarbonylamino-[4-((R)-2-hydroxy-propoxy)-phenyl]-acetic acidHCID 68620103—

반응 단계

Prepared by the same method as described in example 3 except that (i) 2-chloro-4-iodo-aniline was used in place of 4-bromo-2-chloro-aniline in step 1, and (ii) (R)-tert-butoxycarbonylamino-[4-((R)-2-hydroxy-propoxy)-phenyl]-acetic acid was used in place of (R)-tert-butoxycarbonylamino-[4-(2-tert-butoxy-ethoxy)-phenyl]-acetic acid in step 2. (R)-tert-Butoxycarbonylamino-[4-((R)-2-hydroxy-propoxy)-phenyl]-acetic acid was prepared as described in example 48 except that (R)-2-methyl-oxirane was used in place of 2-(2bromo-ethoxy)-tetrahydropyran.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07612212B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-9f20a8e1752c467da7840a1225c65731
출처 메모uspto-grants-2009_11