Реакция #58055

Уравнение реакции

2,3,3a,4-tetrahydro-1H-pyrrolo[2,1-c]-[1,2,4]benzothiadiazin-7-ol 5,5-dioxide

(4-acetylphenyl)boronic acid

pyridine

→

1-{4-[(5,5-Dioxido-2,3,3a,4-tetrahydro-1H-pyrrolo[2,1-c][1,2,4]benzothiadiazin-7-yl)oxy]phenyl}ethanone

Растворители

methylene chloride

methylene chloride

Условия реакции

Обработка

1. 1
   workup.ADDITIONThe reaction mixture is diluted
2. 2
   Фильтрацияthe suspension is filtered
3. 3
   КонцентрированиеThe filtrate is concentrated
4. 4
   Промывкаis eluted with a CH2Cl2/acetone 99/1 system
5. 5
   workup.ADDITIONThe fractions containing the expected product
6. 6
   Другоеevaporated
7. 7
   ФильтрацияAfter filtering off the solid
8. 8
   Другоеthe title product is recovered in the form of white powder

Методика

A suspension composed of 3.0 g (12.48 mmol) of 2,3,3a,4-tetrahydro-1H-pyrrolo[2,1-c]-[1,2,4]benzothiadiazin-7-ol 5,5-dioxide, 3.18 g (18.73 mmol) of (4-acetylphenyl)boronic acid, 3.42 g (18.82 mmol) of copper(II) acetate, 3.03 ml (37.15 mmol) of pyridine and about 500 mg of 4 Å molecular sieve in 150 ml of methylene chloride is stirred overnight. The reaction mixture is diluted by adding a further 100 ml of methylene chloride and the suspension is filtered. The filtrate is concentrated and then directly placed on a silica column which is eluted with a CH2Cl2/acetone 99/1 system. The fractions containing the expected product are combined and evaporated, and the residue is taken up in ethyl ether. After filtering off the solid, the title product is recovered in the form of white powder.

Источник