HRID2359800

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID23149887

2-Bromo-4-(trifluoromethyl)-1,3-thiazole

C4HBrF3NS

结构：CC(C)(C)OC(=O)CN(C(=O)OC(C)(C)C)c1cccc(C(NCc2ccc(B3OC(C)(C)C(C)(C)O3)cc2)S(=O)(=O)c2ccccn2)n1

HCID86651786

未命名化合物

PRODUCTS

生成物

结构：CC(C)(C)OC(=O)CN(C(=O)OC(C)(C)C)c1cccc(C(NCc2ccc(-c3nc(C(F)(F)F)cs3)cc2)S(=O)(=O)c2ccccn2)n1

HCID86651785

未命名化合物

收率 90%

PROCEDURE

实验过程

Reaction and post-treatment were carried out in the same manner as in Example 22-(c) except for using tert-butyl[tert-butoxycarbonyl(6-{(pyridin-2-ylsulfonyl)[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)benzyl]aminomethyl}pyridin-2-yl)amino]acetate (490 mg, containing 0.700 mmol of a pure content) obtained in Example 22-(b), and using 2-bromo-4-trifluoromethylthiazole (see WO 2005/077912A) (341 mg, 1.47 mmol) in place of 2-bromo-5-methylthiazole to afford the title compound (454 mg) as a white foam. (Yield: 90%)

WORKUP

后处理

customReaction
additioncontaining 0.700 mmol of a pure content)
customobtained in Example 22-(b)

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-736299de8ca94c338f8c0acd27cb5463
来源数据集: uspto-grants-2014_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08685986B2
来源说明: uspto-grants-2014_04

反应 SMILES

[C:1]([O:5][C:6](=[O:49])[CH2:7][N:8]([C:42]([O:44][C:45]([CH3:48])([CH3:47])[CH3:46])=[O:43])[C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH:15]([S:33]([C:36]2[CH:41]=[CH:40][CH:39]=[CH:38][N:37]=2)(=[O:35])=[O:34])[NH:16][CH2:17][C:18]2[CH:23]=[CH:22][C:21](B3OC(C)(C)C(C)(C)O3)=[CH:20][CH:19]=2)[N:10]=1)([CH3:4])([CH3:3])[CH3:2].Br[C:51]1[S:52][CH:53]=[C:54]([C:56]([F:59])([F:58])[F:57])[N:55]=1>>[C:1]([O:5][C:6](=[O:49])[CH2:7][N:8]([C:42]([O:44][C:45]([CH3:48])([CH3:47])[CH3:46])=[O:43])[C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH:15]([S:33]([C:36]2[CH:41]=[CH:40][CH:39]=[CH:38][N:37]=2)(=[O:35])=[O:34])[NH:16][CH2:17][C:18]2[CH:19]=[CH:20][C:21]([C:51]3[S:52][CH:53]=[C:54]([C:56]([F:59])([F:58])[F:57])[N:55]=3)=[CH:22][CH:23]=2)[N:10]=1)([CH3:3])([CH3:4])[CH3:2]