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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 489231생성일: 2026년 10월 24일

3-(3,5-Dichlorophenyl)-1-methylimidazolidine-2,4-dione → (1S*,4R*)-1-(4-Bromophenyl)-7-(3,5-dichlorophenyl)-5-methyl-5,7-diazaspiro[3.4]octane-6,8-dione

https://huagongshe.com/ko/reaction/489231

반응식

참여 물질

역할이름HCID투입량
반응물3-(3,5-Dichlorophenyl)-1-methylimidazolidine-2,4-dioneHCID 11994510—
반응물1-Bromo-4-(3-bromo-1-chloropropyl)benzeneHCID 12386248—
생성물(1S*,4R*)-1-(4-Bromophenyl)-7-(3,5-dichlorophenyl)-5-methyl-5,7-diazaspiro[3.4]octane-6,8-dioneHCID 60054870—

반응 단계

Using the same procedure as in Example 1 starting from 1-bromo-4-(3-bromo-1-chloropropyl)benzene (Preparation 7) and 3-(3,5-dichlorophenyl)-1-methylimidazolidine-2,4-dione, the above titled compound was obtained after reverse phase HPLC purification (gradient from CH3CN/H2O/TFA: 5/95/0.05 to CH3CN/H2O/TFA: 80/20/0.05). 1H NMR (CDCl3): 7.44 (2H, d, J=8.4 Hz), 7.25 (1H, m), 6.95-7 (4H, m), 4.05 (1H, t, J=10.1 Hz), 3.22 (3H, s), 2.65-2.85 (1H, br q), 2.4-2.65 (2H, m), 2.1-2.3 (1H, br q).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06977267B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-f1e88edbaf794be7be0d0c8acbb077a8
출처 메모uspto-grants-2005_12