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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30605생성일: 2026년 10월 23일

Diisopropylamine → 2-Amino-5-[4-(difluoromethoxy)phenyl]-5-[3-(5-hydroxypent-1-yn-1-yl)phenyl]-3-methyl-3,5-dihydro-4H-imidazol-4-one

https://huagongshe.com/ko/reaction/30605

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참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물4-Pentyn-1-olHCID 79346—
반응물Tris(1,1-dimethylethyl)phosphineHCID 83681—
반응물2-amino-4-(3-bromophenyl)-4-(4-(difluoromethoxy)phenyl)-1-methyl-1H-imidazol-5(4H)-oneHCID 59790307—
촉매Bis(benzonitrile)palladium chlorideHCID 498840—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물2-Amino-5-[4-(difluoromethoxy)phenyl]-5-[3-(5-hydroxypent-1-yn-1-yl)phenyl]-3-methyl-3,5-dihydro-4H-imidazol-4-oneHCID 5979032373.3%

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온도80 °C

반응 단계

A mixture of 2-amino-5-(3-bromophenyl)-5-[4-(difluoromethoxy)phenyl]-3-methyl-3,5-dihydro-4H-imidazol-4-one (1.15 g, 2.8 mmol), dioxane, bis(benzonitrile)dichloropalladium(II) (32.2 mg, 0.084 mmol), tri-tert-butyl phosphine (10% w/w in hexane, 339 mg, 0.17 mmol) and diisopropyl amine (340 mg, 3.36 mmol) was degassed under argon for 5 minutes, treated with pent-4-yn-1-ol (236 mg, 2.8 mmol), stirred at 80° C. for 5 hours, poured into water and extracted with ethyl acetate. The organic extracts were combined, dried over MgSO4 and concentrated in vacuo. Purification of the resultant residue by ICSO (EtOAc/MeOH 10/1) gave the title compound as a white solid (849 mg), identified by NMR and mass spectral analyses. MS m/e [M+H]+ 414.2

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423158B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-5415d204dca748d18d663fed98bde097
출처 메모uspto-grants-2008_09