Реакция #2348108

ord-d25522b44d8649a587ac5c428f8dee3f

Уравнение реакции

COc1cc(Br)c(Cl)cc1NN
(4-Bromo-5-chloro-2-methoxyphenyl)hydrazine
COc1cc(Br)c(Cl)cc1NN
(4-bromo-5-chloro-2-methoxyphenyl)hydrazine
COc1cc(Br)c(Cl)cc1NN
Intermediate 2
COc1cc(Br)c(Cl)cc1NN
(4-bromo-5-chloro-2-methoxyphenyl)hydrazine
O=C(O)C(=O)c1ccc(Br)s1
2-(5-bromothien-2-yl)glyoxylic acid
CCN(CC)CC
Triethylamine
[N-]=[N+]=NP(=O)(c1ccccc1)c1ccccc1
diphenylphosphorylazide
COc1cc(Br)c(Cl)cc1-n1nc(-c2ccc(Br)s2)[nH]c1=O
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%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe reaction was heated
  2. 2
    Температураat reflux 3-18 hours
  3. 3
    ТемператураAfter cooling to room temperature
  4. 4
    Фильтрацияsolids were filtered
  5. 5
    Промывкаwashed 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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07846671B2uspto-grants-2010_12