Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49984생성일: 2026년 10월 24일
Sodium Iodide → 7-[2-(4-Bromophenyl)ethyl]-2-(3,5-dichlorophenyl)-tetrahydro-imidazo[1,5-a]pyrazine-1,3-dione
https://huagongshe.com/ko/reaction/49984
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4-Bromophenethyl bromide | HCID 11010825 | — |
| 반응물 | 2-(3,5-Dichlorophenyl)-tetrahydro-imidazo[1,5-a]pyrazine-1,3-dione | HCID 21301001 | — |
| 용매 | 3-Methyl-2-butanone | HCID 11251 | — |
| 생성물 | 7-[2-(4-Bromophenyl)ethyl]-2-(3,5-dichlorophenyl)-tetrahydro-imidazo[1,5-a]pyrazine-1,3-dione | HCID 21301014 | — |
반응 단계
A mixture of 1-bromo-4-(2-bromoethyl)benzene (101 mg, 0.38 mmol, prepared as described in Synth.Commun [1996], 26, pp. 1467-1472), 2-(3,5-dichlorophenyl)-tetrahydro-imidazo[1,5-a]pyrazine-1,3-dione (100 mg, 0.33 mmol, Prep. 19), potassium carbonate (48 mg, 0.35 mmol) and sodium iodide (10 mg, 0.06 mmol) in methyl isopropyl ketone (2 mL) was heated at 100° C. for 48 h. The precipitate was discarded and the filtrate was concentrated under vacuum and chromatographed over silica gel (CH2Cl2). The obtained oil was treated with Et2O/HCl to yield the hydrochloride of 7-[2-(4-bromophenyl)ethyl]-2-(3,5-dichlorophenyl)-tetrahydro-imidazo[1,5-a]pyrazine-1,3-dione as a white solid (60 mg). 1H NMR (CDCl3) of the free base: 7.25-7.4 (5H, m), 7.00 (2H, d, J=8.3Hz), 4-4.15 (2H, m), 3.32 (1H, dd, J1=4.1 Hz, J2=11.1 Hz), 3.09 (1H, dt), 2.87 (1H, br d), 2.5-2.8 (4H, m), 1.95-2.15 (2H, m)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06710064B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-6e78110cbfb549ef9b67c2bbe72dedd0 |
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| 출처 메모 | uspto-grants-2004_03 |
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