Reacción #988017

ord-6b1dc8549abb470a880fb9eca942676d

Ecuación de reacción

[Cl-].[Na+]
sodium chloride
CS(=O)(=O)c1nsc(-c2cccc(Cl)c2)n1
3-methylsulfonyl-5-(3-chlorophenyl)-1,2,4-thiadiazole
CCC#CCO
2-pentyne-1-ol
[H-].[Na+]
sodium hydride
CCC#CCOc1nsc(-c2cccc(Cl)c2)n1
5-(3-chlorophenyl)-3-(2-pentynyloxy)-1,2,4-thiadiazole
Rendimiento 81.7%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooling
  2. 2
    workup.STIRRINGfurther stirred at room temperature for 1 hour
  3. 3
    Extracciónthe mixture was extracted with t-butyl methyl ether
  4. 4
    OtroThe residue obtained by concentration of the organic layer

Procedimiento

In 2.5 ml of N,N-dimethylformamide, 350 mg of 3-methylsulfonyl-5-(3-chlorophenyl)-1,2,4-thiadiazole and 117 mg of 2-pentyne-1-ol were dissolved, to the resulting solution was added 56 mg of sodium hydride (60% oily) with ice-cooling, and the mixture was stirred for 30 minutes, and further stirred at room temperature for 1 hour. Then, the reaction mixture was poured into an aqueous saturated sodium chloride solution, and the mixture was extracted with t-butyl methyl ether. The residue obtained by concentration of the organic layer was subjected to silica gel column chromatography to obtain 290 mg of 5-(3-chlorophenyl)-3-(2-pentynyloxy)-1,2,4-thiadiazole (the compound (78) of the present invention).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07361675B2uspto-grants-2008_04