반응식
[B-](F)(F)(F)F.CCOC(C(C#N)=NOC(N(C)C)=[N+](C)C)=O.[NH2:23][C:24]1[CH:29]=[CH:28][C:27]([N:30]2[CH:34]=[CH:33][N:32]([C:35]3[CH:40]=[CH:39][C:38]([O:41][C:42]4[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=4)=[CH:37][CH:36]=3)[C:31]2=[O:48])=[CH:26][CH:25]=1.CCN(C(C)C)C(C)C.[CH3:58][N:59]([CH3:64])[CH2:60][C:61](O)=[O:62]>CN(C=O)C.O>[CH3:58][N:59]([CH3:64])[CH2:60][C:61]([NH:23][C:24]1[CH:25]=[CH:26][C:27]([N:30]2[CH:34]=[CH:33][N:32]([C:35]3[CH:40]=[CH:39][C:38]([O:41][C:42]4[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=4)=[CH:37][CH:36]=3)[C:31]2=[O:48])=[CH:28][CH:29]=1)=[O:62]참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
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.
후처리
- extractionextracted with ethyl acetate
- washThe organic phase was washed with sodium bicarbonate solution
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- customThe residue was purified by preparative HPLC
- customMS (ESI): 429 ([M+H]+) was obtained as hydrotrifluoroacetate in this way
출처 및 근거
- ORD 기록
- ord-2ec5c750372743508bfd8f7ef27ffb95
- 출처 데이터셋
- uspto-grants-2006_11
- 특허 번호
- US07141561B2
연결된 노트
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