Реакция #4269

Уравнение реакции

n-butyl-lithium

5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

2-methyl-4-pentynoic acid chloride

→

desired compound

5,11-Dihydro-11-[1-oxo-2-methyl-4-pentynyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one

Растворители

n-hexane

tetrahydrofuran

tetrahydrofuran

ethyl acetate

Условия реакции

Обработка

1. 1
   workup.STIRRINGTHe mixture is stirred for a further hour at ambient temperature
2. 2
   Температураcooled to 5° to 10° C.
3. 3
   workup.ADDITIONare added dropwise to the reaction solution
4. 4
   workup.STIRRINGThe mixture is stirred for a further 3 hours at ambient temperature
5. 5
   ДругоеThe organic phase is separated off
6. 6
   Экстракцияextracted twice with 500 ml of saturated saline solution
7. 7
   Сушкаdried over magnesium sulphate
8. 8
   Другоеevaporated to dryness in vacuo

Методика

At 0° to 10° C., with stirring, 416 ml (0.65 mol) of an n-butyl-lithium solution in n-hexane are added dropwise to a suspension of 63 g (0.3 mol) of 5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one in 1500 ml of absolute tetrahydrofuran. THe mixture is stirred for a further hour at ambient temperature, then cooled to 5° to 10° C. and this temperature 46.8 g (0.36 mol) of 2-methyl-4-pentynoic acid chloride (not purified) dissolved in 100 ml of absolute tetrahydrofuran are added dropwise to the reaction solution. The mixture is stirred for a further 3 hours at ambient temperature, then added to 2000 ml of a saturated saline solution and diluted with about 2000 ml of ethyl acetate. The organic phase is separated off, extracted twice with 500 ml of saturated saline solution, dried over magnesium sulphate and evaporated to dryness in vacuo. The desired compound is obtained as a brownish-yellow product which is used without further purification in the next step.

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