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1022956-26-8

2-(2,5-dichloropyrimidin-4-ylamino)-N,N-dimethylbenzenesulfonamide synthesis

3synthesis methods
54468-86-9 Synthesis
2-amino-N,N-dimethylbenzenesulfonamide

54468-86-9
68 suppliers
$14.00/100mg

5750-76-5 Synthesis
2,4,5-Trichloropyrimidine

5750-76-5
361 suppliers
$5.00/1g

2-(2,5-dichloropyrimidin-4-ylamino)-N,N-dimethylbenzenesulfonamide

1022956-26-8
6 suppliers
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Yield:1022956-26-8 64%

Reaction Conditions:

with N-ethyl-N,N-diisopropylamine for 12 h;Reflux;

Steps:

4.1.1.12. (2-((2,5-Dichloropyrimidin-4-yl)amino)phenyl)dimethylphosphineoxide (51l).

General procedure: A solution of 2,4,5-trichloropyrimidine(1.82 g, 10 mmol), (2-aminophenyl)dimethylphosphine oxide(1.69 g, 10 mmol) and N,N-diisopropylethylamine (1.94 g, 15 mmol)in propan-2-ol (25 mL) was heated under reflux for 12 h. The solvent was removed by evaporation and the residue was dissolvedin CH2Cl2 (100 mL). The solution was washed with water andsaturated sodium chloride solution and dried, filtered andconcentrated. The residuewas purified by flash chromatography onsilica gel (0e2% MeOH in DCM) to afford compound 51l (1.60 g,50%).

References:

Chen, Yongfei;Wu, Jiaxin;Wang, Aoli;Qi, Ziping;Jiang, Taoshan;Chen, Cheng;Zou, Fengming;Hu, Chen;Wang, Wei;Wu, Hong;Hu, Zhenquan;Wang, Wenchao;Wang, Beilei;Wang, Li;Ren, Tao;Zhang, Shanchun;Liu, Qingsong;Liu, Jing [European Journal of Medicinal Chemistry,2017,vol. 139,p. 674 - 697]

23530-43-0 Synthesis
N,N-dimethyl-2-nitrobenzenesulfonamide

23530-43-0
23 suppliers
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2-(2,5-dichloropyrimidin-4-ylamino)-N,N-dimethylbenzenesulfonamide

1022956-26-8
6 suppliers
inquiry