反应方程式
[CH2:1]([O:8][C:9]([N:11]([CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([C:32]([F:35])([F:34])[F:33])[CH:27]=1)[C:12]1[C:17](=[O:18])[N:16]2[C@H:19]([C:22](O)=[O:23])[CH2:20][CH2:21][C:15]2=[N:14][CH:13]=1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:36]([O:40][C:41](=[O:53])[NH:42][C:43]([C:45]1[CH:50]=[CH:49][C:48]([CH2:51][NH2:52])=[CH:47][CH:46]=1)=[NH:44])([CH3:39])([CH3:38])[CH3:37].C([O-])(O)=O.[Na+].C1C=NC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C>CCOC(C)=O.C(Cl)Cl.CN(C=O)C>[C:36]([O:40][C:41]([NH:42][C:43](=[NH:44])[C:45]1[CH:46]=[CH:47][C:48]([CH2:51][NH:52][C:22]([C@H:19]2[N:16]3[C:17](=[O:18])[C:12]([N:11]([CH2:25][C:26]4[CH:31]=[CH:30][CH:29]=[C:28]([C:32]([F:34])([F:35])[F:33])[CH:27]=4)[C:9](=[O:10])[O:8][CH2:1][C:2]4[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=4)=[CH:13][N:14]=[C:15]3[CH2:21][CH2:20]2)=[O:23])=[CH:49][CH:50]=1)=[O:53])([CH3:39])([CH3:37])[CH3:38]参与物
8
反应物 5
产物 1
试剂、催化剂与溶剂 2
实验过程
To a solution of intermediate 25a (0.281 mmol) and [(4-aminomethyl-phenyl)-imino-methyl]-carbamic acid tert-butyl ester (84 mg, 0.337 mmol) in 3 mL 5:1 CH2Cl2/DMF at 0° C., were added NaHCO3 (59 mg, 0.703 mmol), HOAT (42.1 mg, 0.309 mmol), and EDCI (75.5 mg, 0.393 mmol). The mixture was allowed to warm to rt and stir 20 h, then was diluted with EtOAc. The organic phase was washed with H2O, 1N HCl, H2O, and sat. NaHCO3, and brine, dried (Na2SO4) and brine. The crude residue was triturated with Et2O to afford 160 mg (79%) of intermediate 25b as a white solid. MS (ESI) 719.4 (M+H+).
后处理
- washThe organic phase was washed with H2O, 1N HCl, H2O, and sat. NaHCO3, and brine
- dry with materialdried (Na2SO4) and brine
- customThe crude residue was triturated with Et2O
来源与证据
- ORD记录
- ord-f36da15899fd4af9811f6c580396af9c
- 来源数据集
- uspto-grants-2006_08
- 专利号
- US07094783B2
关联笔记
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