HRID1035414

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID11096760

未命名化合物

结构：Cc1nc2nccc(Oc3ccc(N)c(F)c3)c2[nH]c1=O

HCID46901248

未命名化合物

PRODUCTS

生成物

结构：Cc1nc2nccc(Oc3ccc(NC(=O)Nc4cc(C(C)(C)C)nn4-c4ccccc4)c(F)c3)c2[nH]c1=O

HCID44133545

未命名化合物

PROCEDURE

实验过程

Method F3 was used with 3-tert-butyl-5-isocyanato-1-phenyl-1H-pyrazole and 8-(4-Amino-3-fluorophenoxy)-3-methylpyrido[2,3-b]pyrazin-2(1H)-one.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-bd8974c1d5d4440bac7f60ed7f06a81c
来源数据集: uspto-grants-2013_10
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08546387B2
来源说明: uspto-grants-2013_10

反应 SMILES

[C:1]([C:5]1[CH:9]=[C:8]([N:10]=[C:11]=[O:12])[N:7]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[N:6]=1)([CH3:4])([CH3:3])[CH3:2].[NH2:19][C:20]1[CH:38]=[CH:37][C:23]([O:24][C:25]2[C:34]3[NH:33][C:32](=[O:35])[C:31]([CH3:36])=[N:30][C:29]=3[N:28]=[CH:27][CH:26]=2)=[CH:22][C:21]=1[F:39]>>[C:1]([C:5]1[CH:9]=[C:8]([NH:10][C:11]([NH:19][C:20]2[CH:38]=[CH:37][C:23]([O:24][C:25]3[C:34]4[NH:33][C:32](=[O:35])[C:31]([CH3:36])=[N:30][C:29]=4[N:28]=[CH:27][CH:26]=3)=[CH:22][C:21]=2[F:39])=[O:12])[N:7]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[N:6]=1)([CH3:4])([CH3:2])[CH3:3]