HRID23536

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID4176318

5-tert-Butyl-o-anisidine

C11H17NO

结构：COc1ccc(C(C)(C)C)cc1NC(=O)Nc1ccc(Oc2ccnc(C#N)n2)c2ccccc12

HCID9912417

未命名化合物

HCID57418781

未命名化合物

PRODUCTS

生成物

结构：COC(=O)c1nccc(Oc2ccc(NC(=O)Nc3cc(C(C)(C)C)ccc3OC)c3ccccc23)n1

HCID10278652

未命名化合物

PROCEDURE

实验过程

The title compound was prepared from the above amine and 5-tert-butyl-2-methoxyaniline by the procedure described for 1-(5-tert-butyl-2-methoxy-phenyl)-3-[4-(2-cyano-pyrimidin-4-yloxy)-naphthalen-1-yl]-urea (Example 1).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-724dd17be6c24fe292b9ebef47216276
来源数据集: uspto-grants-2005_02
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06852717B2
来源说明: uspto-grants-2005_02

反应 SMILES

[CH3:1][O:2][C:3]([C:5]1[N:10]=[C:9]([O:11][C:12]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[C:15]([NH2:22])=[CH:14][CH:13]=2)[CH:8]=[CH:7][N:6]=1)=[O:4].C(C1C=CC(OC)=C(C=1)N)(C)(C)C.[C:36]([C:40]1[CH:41]=[CH:42][C:43]([O:69][CH3:70])=[C:44]([NH:46][C:47](NC2C3C(=CC=CC=3)C(OC3C=CN=C(C#N)N=3)=CC=2)=[O:48])[CH:45]=1)([CH3:39])([CH3:38])[CH3:37]>>[CH3:1][O:2][C:3]([C:5]1[N:10]=[C:9]([O:11][C:12]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[C:15]([NH:22][C:47]([NH:46][C:44]3[CH:45]=[C:40]([C:36]([CH3:37])([CH3:39])[CH3:38])[CH:41]=[CH:42][C:43]=3[O:69][CH3:70])=[O:48])=[CH:14][CH:13]=2)[CH:8]=[CH:7][N:6]=1)=[O:4]