HRID2270425

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7728

5-Ethyl-2-methylpyridine

C8H11N

结构：CCS(=O)(=O)Nc1cc(-n2c(=O)cc(C(F)(F)F)n(C)c2=O)c(F)cc1Br

HCID10874406

未命名化合物

PRODUCTS

生成物

结构：CCS(=O)(=O)Nc1cc(-n2c(=O)cc(C(F)(F)F)n(C)c2=O)c(F)cc1C#N

HCID11091077

未命名化合物

收率 94%

AUXILIARIES

试剂、催化剂与溶剂

催化剂HCID11186

Zinc cyanide (Zn(CN)2)

C2N2Zn

结构：c1ccc([P](c2ccccc2)(c2ccccc2)[Pd]([P](c2ccccc2)(c2ccccc2)c2ccccc2)([P](c2ccccc2)(c2ccccc2)c2ccccc2)[P](c2ccccc2)(c2ccccc2)c2ccccc2)cc1

催化剂HCID178418397

未命名化合物

CONDITIONS

反应条件

温度: 80 °C

PROCEDURE

实验过程

2.0 g (4.2 mmol) of 3-(4-bromo-5-ethylsulfonylamino-2-fluorophenyl)-1-methyl-6-trifluoromethyl-2,4(1H,3H)pyrimidinedione, 0.3 g of zinc cyanide and 0.5 g of tetrakis(triphenylphosphine)palladium were added to 10 g of 5-ethyl-2-picoline and the mixture was stirred at 80° C. under an argon atmosphere for 3.5 hours. After the reaction was completed, 94% of the title compound was detected as the relative area value in liquid chromatography.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-b1b3968d0611457197dc30ea996ab31b
来源数据集: uspto-grants-2001_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06331628B1
来源说明: uspto-grants-2001_12

反应 SMILES

Br[C:2]1[C:7]([NH:8][S:9]([CH2:12][CH3:13])(=[O:11])=[O:10])=[CH:6][C:5]([N:14]2[C:19](=[O:20])[CH:18]=[C:17]([C:21]([F:24])([F:23])[F:22])[N:16]([CH3:25])[C:15]2=[O:26])=[C:4]([F:27])[CH:3]=1.C(C1C=C[C:33](C)=[N:34]C=1)C>[C-]#N.[Zn+2].[C-]#N.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[C:33]([C:2]1[C:7]([NH:8][S:9]([CH2:12][CH3:13])(=[O:11])=[O:10])=[CH:6][C:5]([N:14]2[C:19](=[O:20])[CH:18]=[C:17]([C:21]([F:22])([F:23])[F:24])[N:16]([CH3:25])[C:15]2=[O:26])=[C:4]([F:27])[CH:3]=1)#[N:34]