反应 #1350594

ord-293ef6d524064eb3bf4c40e69bbc5979

反应方程式

ClCCCl
EDC
CNc1nc2c(C)c(C(=O)O)ccc2s1
2-methylamino-4-methylbenzothiazole-5-carboxylic acid
Cn1nccc1O
1-methyl-5-hydroxypyrazole
CC#N
acetonitrile
CNc1nc2c(C)c(C(=O)Oc3ccnn3C)ccc2s1
1-Methylpyrazol-5-yl 2-Methylamino-4-methylbenzothiazole-5-carboxylate

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取the mixture was extracted with ethyl acetate
  2. 2
    洗涤The organic phase was washed
  3. 3
    其他dried
  4. 4
    其他the product was then purified by crystallization

实验过程

3.1 g of 2-methylamino-4-methylbenzothiazole-5-carboxylic acid (0.014 mol) and 1.4 g of 1-methyl-5-hydroxypyrazole (0.015 mol) were dissolved in 110 ml of abs. acetonitrile and admixed with 2.67 g of EDC (0.014 mol), 1,2 ml of triethylamine and a catalytic amount of DMAP. After the reaction had ended, the solution was poured into water and the mixture was extracted with ethyl acetate. The organic phase was washed and dried, and the product was then purified by crystallization. Yield: 2.2 g (52%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06541423B1uspto-grants-2003_04