HRID2042846

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID12734

Diisopropylcarbodiimide

C7H14N2

HCID56840195

未命名化合物

结构：Nc1cc(C(=O)N[C@H]2CC[C@H](C(F)(F)F)CC2)c(OCC(F)F)nc1N

HCID178507778

未命名化合物

PRODUCTS

生成物

结构：Cc1ccc(CNC(=O)C(C)(C)C)c(C)c1Nc1nc2nc(OCC(F)F)c(C(=O)N[C@H]3CC[C@H](C(F)(F)F)CC3)cc2[nH]1

HCID178425578

未命名化合物

PROCEDURE

实验过程

The title compound is prepared from N-(2,4-dimethyl-3-isothiocyanato-benzyl)-2,2-dimethyl-propionamide (65 mg, 0.24 mmol) and 5,6 diamino-2-(2,2-difluoro-ethoxy)-N-(trans-4-trifluoromethyl-cyclohexyl)-nicotinamide (90 mg, 0.24 mmol) with DIC in analogy to examples 8a/8b.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-2d9a0f0f64a64376935faeee970e5448
来源数据集: uspto-grants-2013_11
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08586604B2
来源说明: uspto-grants-2013_11

反应 SMILES

[CH3:1][C:2]1[C:15]([N:16]=[C:17]=S)=[C:14]([CH3:19])[CH:13]=[CH:12][C:3]=1[CH2:4][NH:5][C:6](=[O:11])[C:7]([CH3:10])([CH3:9])[CH3:8].[NH2:20][C:21]1[C:22]([NH2:45])=[N:23][C:24]([O:40][CH2:41][CH:42]([F:44])[F:43])=[C:25]([CH:39]=1)[C:26]([NH:28][C@H:29]1[CH2:34][CH2:33][C@H:32]([C:35]([F:38])([F:37])[F:36])[CH2:31][CH2:30]1)=[O:27].CC(C)N=C=NC(C)C>>[CH3:1][C:2]1[C:15]([NH:16][C:17]2[NH:20][C:21]3[C:22]([N:45]=2)=[N:23][C:24]([O:40][CH2:41][CH:42]([F:44])[F:43])=[C:25]([C:26](=[O:27])[NH:28][C@H:29]2[CH2:30][CH2:31][C@H:32]([C:35]([F:37])([F:36])[F:38])[CH2:33][CH2:34]2)[CH:39]=3)=[C:14]([CH3:19])[CH:13]=[CH:12][C:3]=1[CH2:4][NH:5][C:6](=[O:11])[C:7]([CH3:10])([CH3:9])[CH3:8]