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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 489232생성일: 2026년 10월 23일

3-(3,5-Dichlorophenyl)-1-methylimidazolidine-2,4-dione → (5R*,6S*)-6-(4-Bromophenyl)-3-(3,5-dichlorophenyl)-1-methyl-1,3-diazaspiro[4.5]decane-2,4-dione

https://huagongshe.com/ko/reaction/489232

반응식

참여 물질

역할이름HCID투입량
반응물3-(3,5-Dichlorophenyl)-1-methylimidazolidine-2,4-dioneHCID 11994510—
반응물1-Bromo-4-(1,5-dibromopentyl)benzeneHCID 22025299—
생성물(5R*,6S*)-6-(4-Bromophenyl)-3-(3,5-dichlorophenyl)-1-methyl-1,3-diazaspiro[4.5]decane-2,4-dioneHCID 60054879—

반응 단계

Using the same procedure as in Example 1 starting from 1-bromo-4-(1,5-dibromopentyl)benzene (4.2 g, 10.9 mmol) (Preparation 14) and 3-(3,5-dichlorophenyl)-1-methylimidazolidine-2,4-dione (2.59 g, 10 mmol), the above titled compound was obtained as a white solid (3.1 g, mp=118° C.). 1H NMR (CDCl3): 7.41 (2H, d, J=8.4 Hz), 7.30 (1H, m), 7.00 (2H, d, J=8.4 Hz), 6.90 (2H, m), 3.03 (3H, s), 2.91 (1H, dd, J1=12.9 Hz, J2=3.6 Hz), 2.55 (1H, dq), 2.1-2.3 (1H, m), 1.8-2.05 (5H, m), 1.3-1.6 (1 H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06977267B2
출처 데이터셋uspto-grants-2005_12
ORD IDord-5dbb9c049ebe4bf8bcaa59125ef2285e
출처 메모uspto-grants-2005_12