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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 237928생성일: 2026년 10월 23일

2-Bromopyrimidine → (S)-tert-Butyl 2-(5-(4'-(2-((S)-1-((S)-3-methyl-2-(pyrimidin-2-ylamino)butanoyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)biphenyl-4-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate

https://huagongshe.com/ko/reaction/237928

반응식

참여 물질

역할이름HCID투입량
반응물2-BromopyrimidineHCID 78345—
반응물DiisopropylethylamineHCID 81531—
반응물(S)-tert-butyl 2-(5-(4'-(2-((S)-1-((s)-2-amino-3-methylbutanoyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)biphenyl-4-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylateHCID 59166546—
용매Dimethylsulfoxide tolueneHCID 22340214—
생성물(S)-tert-Butyl 2-(5-(4'-(2-((S)-1-((S)-3-methyl-2-(pyrimidin-2-ylamino)butanoyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)biphenyl-4-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylateHCID 59166544110.8%

반응 조건

온도90 °C

반응 단계

A mixture of (S)-tert-butyl 2-(5-(4′-(2-((S)-1-((S)-2-amino-3-methylbutanoyl)pyrrolidin-2-yl)-1H-imidazol-5-yl)biphenyl-4-yl)-1H-imidazol-2-yl)pyrrolidine-1-carboxylate (cj-2) (0.45 g, 0.72 mmol), 2-bromopyrimidine (0.37 g, 2.34 mmol) and iPr2NEt (0.20 mL, 1.18 mmol) in toluene-DMSO (4:1, 5 mL) was heated at 90° C. overnight. The volatiles were removed in vacuo and the residue was purified by preparative HPLC YMC Pack C-18, 30×100 mm/MeCN—H2O-TFA). The title compound (0.56 g, 74%), as its TFA salt, was obtained as a yellow-orange glass.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642025B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-5c1cc8256fb449068810a482411a8be0
출처 메모uspto-grants-2014_02