Реакция #6313

ord-5d6c2380db7048b1ba438d1bba8589f6

Уравнение реакции

C1CCOC1
tetrahydrofuran
[Br][Mg][CH]1CC1
cyclopropyl magnesium bromide
[Mg]
magnesium
BrC1CC1
cyclopropyl bromide
C1CCOC1
tetrahydrofuran
C1CCOC1
tetrahydrofuran
CN1Cc2c(C=O)ncn2-c2ccncc2C1=O
5,6-dihydro-5-methyl-6-oxo-4H-imidazo [1,5-a]-pyrido [3,4-f][1,4]-diazepine-3-carboxaldehyde
OC(C1=CNc2ccncc2C=N1)C1CC1
pyrido-[3,4-f][1,4]-diazepin-3-yl cyclopropyl carbinol

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe reaction was quenched with aqueous ammonium chloride
  2. 2
    Экстракцияextracted with dichloromethane

Методика

To a solution of cyclopropyl magnesium bromide in dry tetrahydrofuran (prepared from 72 mg (3 mmole)) of magnesium and 362 mg (3 mmole) of cyclopropyl bromide in 4 ml of tetrahydrofuran was added at room temperature in one portion a suspension of 240 mg (1 mmole)of 5,6-dihydro-5-methyl-6-oxo-4H-imidazo [1,5-a]-pyrido [3,4-f][1,4]-diazepine-3-carboxaldehyde suspended in a mixture of 1 ml of tetrahydrofuran and 1 ml of hexamethyl-phosphoramide. After 1 hour, the reaction was quenched with aqueous ammonium chloride and extracted with dichloromethane. Column chromatography (SiO2 -5% methanol in dichloromethane) yielded 120 mg of 5,6-dihydro-5-methyl-6-oxo-4H-imidazo-1,5-a]-pyrido-[3,4-f][1,4]-diazepin-3-yl cyclopropyl carbinol as an oil, (43%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05247079uspto-grants-1993_09