HRID1084995

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID3311515

未命名化合物

结构：CC(=O)O.CNC(=O)[C@H](CC(C)C)NC(=O)C(CC(C)C)CP(=O)(CN)OC

HCID86743557

未命名化合物

PRODUCTS

生成物

结构：CNC(=O)[C@H](CC(C)C)NC(=O)C(CC(C)C)CP(=O)(CN1C(=O)c2c(C)ccc(OC)c2C1=O)OC

HCID53651813

未命名化合物

收率 47.1%

PROCEDURE

实验过程

In a manner analogous to that described in Example 3(A), from 0.41 g of (aminomethyl)[(RS)-4-methyl-2-[[(S)-3-methyl-1-(methylcarbamoyl)butyl]carbamoyl]pentyl]phosphinic acid methyl ester acetate and 0.21 g of 3-methyl-6-methoxyphthalic anhydride there was obtained 0.245 g of [(3-methoxy-6-methylphthalimido)methyl][(RS)-4-methyl-2-[[(S)-3-methyl-1-(methylcarbamoyl)butyl]carbamoyl]pentyl]phosphinic acid methyl ester in the form of a white foam.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-bbf7ba86e4fb44269e0daf5ab30a674e
来源数据集: uspto-grants-1991_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05006651
来源说明: uspto-grants-1991_04

反应 SMILES

C(O)(=O)C.[CH3:5][O:6][P:7]([CH2:27][NH2:28])([CH2:9][CH:10]([C:15](=[O:26])[NH:16][C@H:17]([C:22](=[O:25])[NH:23][CH3:24])[CH2:18][CH:19]([CH3:21])[CH3:20])[CH2:11][CH:12]([CH3:14])[CH3:13])=[O:8].[CH3:29][C:30]1[CH:40]=[CH:39][C:38]([O:41][CH3:42])=[C:32]2[C:33]([O:35][C:36](=O)[C:31]=12)=[O:34]>>[CH3:5][O:6][P:7]([CH2:27][N:28]1[C:33](=[O:34])[C:32]2=[C:38]([O:41][CH3:42])[CH:39]=[CH:40][C:30]([CH3:29])=[C:31]2[C:36]1=[O:35])([CH2:9][CH:10]([C:15](=[O:26])[NH:16][C@H:17]([C:22](=[O:25])[NH:23][CH3:24])[CH2:18][CH:19]([CH3:21])[CH3:20])[CH2:11][CH:12]([CH3:14])[CH3:13])=[O:8]