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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 561988생성일: 2026년 10월 27일

Chlorosuccinimide → (R)-3-{(S)-2-(4-Fluoro-phenyl)-1-[5-(4-iodo-phenyl)-1H-imidazol-2-yl]-ethyl}-5-[4-(2-hydroxy-ethoxy)-phenyl]-imidazolidine-2,4-dione

https://huagongshe.com/reaction/561988

반응식

참여 물질

역할이름HCID투입량
반응물ChlorosuccinimideHCID 31398—
반응물1-(4-Iodophenyl)ethan-1-oneHCID 72869—
반응물3-((R)-1-{(S)-1-[5-(4-iodo-phenyl)-1H-imidazol-2-yl]-2-methyl-propyl}-2,5-dioxo-imidazolidin-4-yl)-propionic acidHCID 57771978—
반응물(R)-tert-butoxycarbonylamino-(4-dimethylcarbamoylmethoxy-phenyl)-acetic acidHCID 66815126—
반응물{(1S,2S)-1-[5-(2-fluoro-phenyl)-1H-imidazol-2-yl]-2-phenyl-propyl}-carbamic acid tert-butyl esterHCID 67001749—
생성물(R)-3-{(S)-2-(4-Fluoro-phenyl)-1-[5-(4-iodo-phenyl)-1H-imidazol-2-yl]-ethyl}-5-[4-(2-hydroxy-ethoxy)-phenyl]-imidazolidine-2,4-dioneHCID 57771867—

반응 단계

Prepared by the same method as described in example 1 except that (i) steps A, B, and C were omitted; (ii) commercially available 1-(4-iodo-phenyl)-ethanone was used in place of 1-(2-fluoro-4-iodo-phenyl)-ethanone in step 41-D; (iii) (S)-2-tert-butoxycarbonylamino-3-(4-fluoro-phenyl)-propionic acid was used in place of (2S,3S)-2-tert-butoxycarbonylamino-3-phenyl-butyric acid in step 41-E and (iv) chlorination of the 5-position of the imidazole ring with N-chlorosuccinimide in step 41-F was omitted. HR-MS: calcd for C28H24FlN4O4 [M+H+] 627.0899. Found 627.0904.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063085B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-4a6606d151b5474a88f9efc72fdba03d
출처 메모uspto-grants-2011_11