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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 548169생성일: 2026년 10월 25일

1-(2-Bromoethyl)-3-fluorobenzene → 3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)-1-(3-fluorophenethyl)imidazolidine-2,4-dione

https://huagongshe.com/reaction/548169

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참여 물질

역할이름HCID투입량
반응물1-(2-Bromoethyl)-3-fluorobenzeneHCID 573129—
반응물3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)imidazolidine-2,4-dioneHCID 57422424—
생성물3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)-1-(3-fluorophenethyl)imidazolidine-2,4-dioneHCID 5794494922%

반응 단계

Prepared as in example 10-52 from 3-(1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazol-4-yl)imidazolidine-2,4-dione (example 10-1) and 3-fluorophenethyl bromide. Yield: 22%. 1H NMR (DMSO-d6, 400 MHz): δ2.11 (s, 3H), 2.38 (s, 3H), 2.80 (t, J=7.2 Hz, 2H), 3.57 (t, J=7.2 Hz, 2H), 4.06 (s, 2H), 5.17 (s, 2H), 6.85 (dt, J=8.4, 2.0 Hz, 1H), 7.11 (t, J=8.4 Hz, 2H), 7.32 (q, J=7.8 Hz, 1H), 7.73 (s, 1H), 8.12 (s, 1H). MS M+H calculated 398.2; found 398.1. Melting point: 110-111° C. The title compound was shown to inhibit hT2R08 bitter receptor and had an IC50 of 0.06 μM.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07939671B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-34d9b832654a4a2aa7637662358f7f40
출처 메모uspto-grants-2011_05