反应 #1350592

ord-a509b02e3a3f405cbd0d8736dc9d3848

反应方程式

O=N[O-].[Na+]
NaNO2
COC(=O)c1ccc2sc(N)nc2c1C
methyl 2-amino-4-methylbenzothiazole-5-carboxylate
[K+].[OH-]
KOH
Cl
HCl
Cc1c(C(=O)O)ccc2snnc12
4-Methylbenzothiadiazole-5-carboxylic Acid

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他at 0-10° C
  2. 2
    萃取extracted with ethyl acetate
  3. 3
    洗涤The extract was washed
  4. 4
    其他dried
  5. 5
    其他the product was obtained

实验过程

5 g of methyl 2-amino-4-methylbenzothiazole-5-carboxylate (0.02 mol) in 28.6 g of 50% strength KOH were stirred at 120° C. for 4 h. The mixture was then neutralized with 10% strength HCl and admixed with an excess of 40% strength NaNO2 solution at 0-10° C. The reaction mixture was acidified and extracted with ethyl acetate. The extract was washed and dried, and the product was obtained by stripping off the solvent. Yield: 1.3 g (28%).

来源

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