반응식
[CH2:1]([N:4]([C:18]([O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[O:19])[C:5]1[C:10](=[O:11])[N:9]2[C@H:12]([C:15]([OH:17])=O)[CH2:13][CH2:14][C:8]2=[N:7][CH:6]=1)[CH:2]=[CH2:3].[NH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1.C1C=NC2N(O)N=NC=2C=1.C([O-])(O)=O.[Na+].CCN=C=NCCCN(C)C>CCOC(C)=O.C(Cl)Cl.CN(C=O)C>[CH2:21]([O:20][C:18](=[O:19])[N:4]([CH2:1][CH:2]=[CH2:3])[C:5]1[C:10](=[O:11])[N:9]2[C@H:12]([C:15](=[O:17])[NH:28][C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)[CH2:13][CH2:14][C:8]2=[N:7][CH:6]=1)[C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1참가 물질
8
반응물 5
생성물 1
시약·촉매·용매 2
실험 절차
To a solution of 18a (5.50 g, 14.89 mmol) and aniline (1.93 mL, 22.3 mmol) in 75 mL 5:1 CH2Cl2/DMF at 0° C., was added HOAT (2.23 g, 16.4 mmol), NaHCO3 (2.50 g, 29.8 mmol), and EDCI (4.00 g, 20.8 mmol). The mixture was stirred and allowed to warm to rt over 72 h. The reaction was diluted with EtOAc and the organic phase was washed with H2O, 1N HCl, H2O, and brine. The organic phase was dried (Na2SO4) and concentrated. The residue obtained was purified by flash chromatography (80 to 90% EtOAc/hexanes) to afford 3.825 g (58%, 2 steps) of 18b as an off-white solid.
후처리
- washthe organic phase was washed with H2O, 1N HCl, H2O, and brine
- dry with materialThe organic phase was dried (Na2SO4)
- concentrationconcentrated
- customThe residue obtained
- customwas purified by flash chromatography (80 to 90% EtOAc/hexanes)
출처 및 근거
- ORD 기록
- ord-3893d05062934c729de80100e116eee3
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07094783B2
연결된 노트
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