HRID1418145

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID19348606

2-t-Butyl-5-carbamoylaniline

C11H16N2O

结构：CCCCCC(CC(=O)O)c1cc(C(=O)OC)c(OC)cc1OC

HCID19348732

未命名化合物

PRODUCTS

生成物

结构：CCCCCC(CC(=O)Nc1cc(C(N)=O)ccc1C(C)(C)C)c1cc(C(=O)OC)c(OC)cc1OC

HCID19348499

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID21881112

未命名化合物

PROCEDURE

实验过程

Following a similar procedure to that described in Example 44, but using 3-(2,4-dimethoxy-5-methoxycarbonylphenyl)octanoic acid (prepared as described in Preparation 37) and 2-t-butyl-5-carbamoylaniline (prepared as described in Preparation 38), the title compound was obtained as crystals, melting at 101°-103° C. (from methylene chloride-diethyl ether).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-567d043ac886467cabef4ebe8fba37ac
来源数据集: uspto-grants-1999_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05880147
来源说明: uspto-grants-1999_03

反应 SMILES

[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[C:6]([C:11]([O:13][CH3:14])=[O:12])=[CH:5][C:4]=1[CH:15]([CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH2:16][C:17]([OH:19])=O.[C:25]([C:29]1[CH:35]=[CH:34][C:33]([C:36](=[O:38])[NH2:37])=[CH:32][C:30]=1[NH2:31])([CH3:28])([CH3:27])[CH3:26]>C(Cl)Cl.C(OCC)C>[C:25]([C:29]1[CH:35]=[CH:34][C:33]([C:36](=[O:38])[NH2:37])=[CH:32][C:30]=1[NH:31][C:17](=[O:19])[CH2:16][CH:15]([C:4]1[CH:5]=[C:6]([C:11]([O:13][CH3:14])=[O:12])[C:7]([O:9][CH3:10])=[CH:8][C:3]=1[O:2][CH3:1])[CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])([CH3:28])([CH3:26])[CH3:27]