HRID1457585

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID14349

Glycine, N-[(phenylmethoxy)carbonyl]-

C10H11NO4

结构：COc1cc(NC(=O)N(c2ccc(N(C)C)cc2)C2CCCCCC2)c(O)c(C(C)(C)C)c1

HCID10004070

未命名化合物

PRODUCTS

生成物

结构：COc1cc(NC(=O)N(c2ccc(N(C)C)cc2)C2CCCCCC2)c(OC(=O)CNC(=O)OCc2ccccc2)c(C(C)(C)C)c1

HCID22441913

未命名化合物

PROCEDURE

实验过程

2-[3-Cycloheptyl-3-(4-dimethylaminophenyl)ureido]-4-methoxy-6-tert-butylphenol and N-benzyloxycarbonylglycine were treated in the same manner as described in Example 172 (1) to give O-(N-benzyloxycarbonylglycyl)-2-[3-cycloheptyl-3-(4-dimethylaminophenyl)ureido]-4-methoxy-6-tert-butylphenol.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-5be8888e48c84a1e9c2965c51c121023
来源数据集: uspto-grants-1998_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05849732
来源说明: uspto-grants-1998_12

反应 SMILES

[CH:1]1([N:8]([C:25]2[CH:30]=[CH:29][C:28]([N:31]([CH3:33])[CH3:32])=[CH:27][CH:26]=2)[C:9](=[O:24])[NH:10][C:11]2[CH:16]=[C:15]([O:17][CH3:18])[CH:14]=[C:13]([C:19]([CH3:22])([CH3:21])[CH3:20])[C:12]=2[OH:23])[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:34]([O:41][C:42]([NH:44][CH2:45][C:46](O)=[O:47])=[O:43])[C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1>>[CH2:34]([O:41][C:42]([NH:44][CH2:45][C:46]([O:23][C:12]1[C:13]([C:19]([CH3:22])([CH3:21])[CH3:20])=[CH:14][C:15]([O:17][CH3:18])=[CH:16][C:11]=1[NH:10][C:9]([N:8]([CH:1]1[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1)[C:25]1[CH:30]=[CH:29][C:28]([N:31]([CH3:33])[CH3:32])=[CH:27][CH:26]=1)=[O:24])=[O:47])=[O:43])[C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1