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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 723374생성일: 2026년 10월 25일

N,N-Dimethylglycine → 2-Dimethylamino-N-{4-[2-oxo-3-(4-phenoxyphenyl)-2,3-dihydroimidazol-1-yl]phenyl}acetamide

https://huagongshe.com/reaction/723374

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylglycineHCID 673—
반응물DiisopropylethylamineHCID 81531—
반응물O-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733286—
반응물1-(4-Aminophenyl)-3-(4-phenoxyphenyl)-1,3-dihydroimidazol-2-oneHCID 10246828—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-Dimethylamino-N-{4-[2-oxo-3-(4-phenoxyphenyl)-2,3-dihydroimidazol-1-yl]phenyl}acetamideHCID 21873497—

반응 단계

TOTU (327 mg) was added to a solution of 1-(4-aminophenyl)-3-(4-phenoxyphenyl)-1,3-dihydroimidazol-2-one (343 mg) in DMF (3 ml) at 0° C. After 10 minutes, Hünig base (130 mg) and then a solution of dimethylglycine (103 mg) in DMF (1 ml) was added. After a reaction time of 12 hours at room temperature, the mixture was mixed with water and extracted with ethyl acetate. The organic phase was washed with sodium bicarbonate solution, dried over magnesium sulfate and concentrated. The residue was purified by preparative HPLC. The product with the molecular weight of 428.50 (C25H24N4O3); MS (ESI): 429 ([M+H]+) was obtained as hydrotrifluoroacetate in this way.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141561B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-2ec5c750372743508bfd8f7ef27ffb95
출처 메모uspto-grants-2006_11