HRID2392680

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：Cc1nc(-c2ccc(-c3ccc(C(=O)O)cc3)c(C)c2)no1

HCID11130168

未命名化合物

HCID11357613

3-[2-[Bis(1-methylethyl)amino]ethoxy]-4-methoxybenzenamine

C15H26N2O2

PRODUCTS

生成物

结构：COc1ccc(NC(=O)c2ccc(-c3ccc(-c4noc(C)n4)cc3C)cc2)cc1OCCN(C(C)C)C(C)C

HCID18672736

未命名化合物

PROCEDURE

实验过程

The title compound was prepared from 2'-methyl-4'-(5-methyl-1,2,4-oxadiazol-3-yl)biphenyl-4-carboxylic acid (EP 0533268 A1) and 3-(2-diisopropylaminoethoxy)-4-methoxyaniline (D4) following a procedure similar to that described in Example 1 (27%) mp 130°-131° C.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-6c1a9fe6c7df48c4b3fb8dd28175762d
来源数据集: uspto-grants-1998_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05801170
来源说明: uspto-grants-1998_09

反应 SMILES

[CH3:1][C:2]1[CH:7]=[C:6]([C:8]2[N:12]=[C:11]([CH3:13])[O:10][N:9]=2)[CH:5]=[CH:4][C:3]=1[C:14]1[CH:19]=[CH:18][C:17]([C:20](O)=[O:21])=[CH:16][CH:15]=1.[CH:23]([N:26]([CH:39]([CH3:41])[CH3:40])[CH2:27][CH2:28][O:29][C:30]1[CH:31]=[C:32]([CH:34]=[CH:35][C:36]=1[O:37][CH3:38])[NH2:33])([CH3:25])[CH3:24]>>[CH:39]([N:26]([CH:23]([CH3:24])[CH3:25])[CH2:27][CH2:28][O:29][C:30]1[CH:31]=[C:32]([NH:33][C:20]([C:17]2[CH:16]=[CH:15][C:14]([C:3]3[CH:4]=[CH:5][C:6]([C:8]4[N:12]=[C:11]([CH3:13])[O:10][N:9]=4)=[CH:7][C:2]=3[CH3:1])=[CH:19][CH:18]=2)=[O:21])[CH:34]=[CH:35][C:36]=1[O:37][CH3:38])([CH3:41])[CH3:40]