HRID382167

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC(C)(C)[C@H](NC(=O)[C@@H](CC(=O)OCc1ccccc1)n1ccc(-c2ccc(-c3ccc(C(N)=O)cc3)cc2)c1)C(=O)Nc1ccncc1

HCID15459680

未命名化合物

PRODUCTS

生成物

结构：CC(C)(C)[C@H](NC(=O)[C@@H](CC(=O)O)n1ccc(-c2ccc(-c3ccc(C(N)=O)cc3)cc2)c1)C(=O)Nc1ccncc1

HCID54440083

未命名化合物

收率 81%

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID21584119

未命名化合物

PROCEDURE

实验过程

According to the procedure described in Example 5(a), 3(R)-[3-(4′-carbamoylbiphenyl-4-yl)-1H-pyrrol-1-yl]-N-[2,2-dimethyl-1(S)-(N-(pyridin-4-yl)carbamoyl)propyl]succinamic acid benzyl ester was hydrogenolyzed in MeOH/EtOAc to provide 35 mg (81%) of 3(R)-[3-(4′-carbamoylbiphenyl-4-yl)-1H-pyrrol-1-yl]-N-[2,2-dimethyl-1(S)-(N-(pyridin-4-yl)carbamoyl)propyl]succinamic acid as a yellow solid, mp 194-6° C.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-fbee6de917564c949aee7961fa8ef8b9
来源数据集: uspto-grants-2001_10
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06306892B1
来源说明: uspto-grants-2001_10

反应 SMILES

C([O:8][C:9](=[O:49])[CH2:10][C@@H:11]([N:29]1[CH:33]=[CH:32][C:31]([C:34]2[CH:39]=[CH:38][C:37]([C:40]3[CH:45]=[CH:44][C:43]([C:46](=[O:48])[NH2:47])=[CH:42][CH:41]=3)=[CH:36][CH:35]=2)=[CH:30]1)[C:12]([NH:14][C@H:15]([C:20](=[O:28])[NH:21][C:22]1[CH:27]=[CH:26][N:25]=[CH:24][CH:23]=1)[C:16]([CH3:19])([CH3:18])[CH3:17])=[O:13])C1C=CC=CC=1>CO.CCOC(C)=O>[C:46]([C:43]1[CH:42]=[CH:41][C:40]([C:37]2[CH:36]=[CH:35][C:34]([C:31]3[CH:32]=[CH:33][N:29]([C@@H:11]([C:12]([NH:14][C@H:15]([C:20](=[O:28])[NH:21][C:22]4[CH:23]=[CH:24][N:25]=[CH:26][CH:27]=4)[C:16]([CH3:18])([CH3:19])[CH3:17])=[O:13])[CH2:10][C:9]([OH:49])=[O:8])[CH:30]=3)=[CH:39][CH:38]=2)=[CH:45][CH:44]=1)(=[O:48])[NH2:47]