Реакция #2348108
ord-d25522b44d8649a587ac5c428f8dee3f
Уравнение реакции
(4-Bromo-5-chloro-2-methoxyphenyl)hydrazine
(4-bromo-5-chloro-2-methoxyphenyl)hydrazine
Intermediate 2
(4-bromo-5-chloro-2-methoxyphenyl)hydrazine
2-(5-bromothien-2-yl)glyoxylic acid
Triethylamine
diphenylphosphorylazide
→
2-(4-bromo-5-chloro-2-methoxyphenyl)-2,4-dihydro-5-(5-bromothien-2-yl)-3H-1,2,4-triazol-3-one
Выход 75.0%
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Температураthe reaction was heated
- 2Температураat reflux 3-18 hours
- 3ТемператураAfter cooling to room temperature
- 4Фильтрацияsolids were filtered
- 5Промывкаwashed with acetonitrile and ether
Методика
(4-Bromo-5-chloro-2-methoxyphenyl)hydrazine (Intermediate 2) (5.0 g) and 2-(5-bromothien-2-yl)glyoxylic acid (4.7 g) were refluxed in acetonitrile (15-25 ml/mmol starting material) for 30-60 minutes. The reaction was cooled to room temperature. Triethylamine (2.22 g) and diphenylphosphorylazide (6.05 g) were added, and the reaction was heated at reflux 3-18 hours. After cooling to room temperature, solids were filtered and washed with acetonitrile and ether to yield (75%) 2-(4-bromo-5-chloro-2-methoxyphenyl)-2,4-dihydro-5-(5-bromothien-2-yl)-3H-1,2,4-triazol-3-one (Intermediate 3).