تفاعل #63760
ord-b0d496cdc8f24d358b2f6b672a2dde63
معادلة التفاعل
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىis evaporated in vacuo
- 2أخرىThe residue is crystallized from tert.butyl methyl ether/ether
الإجراء التجريبي
3.39 g of 2-[[(3-methyl-2-pyridyl)methyl]sulphinyl]-5-(trifluoromethyl)benzimidazole are dissolved in 50 ml of tetrahydrofuran and treated with 0.77 g of cysteamine. 40 ml of 3N hydrochloric acid are added at an internal temperature of 40°. After stirring at 40° for 10 minutes and at room temperature overnight the mixture is evaporated in vacuo. The residue is crystallized from tert.butyl methyl ether/ether. There is obtained 2-[[(2-aminoethyl)dithio]methyl]-3 -methyl-1-[5-(trifluoromethyl)-2-benzimidazolyl1pyridinium chloride of melting point 95°-100°.