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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6217Erstellt: 23. Oktober 2026

Tetrahydrofuran → Pyrido-[3,4-f][1,4]-diazepin-3-yl cyclopropyl carbinol

https://huagongshe.com/de/reaction/6217

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktBromocyclopropaneHCID 78037—
EduktMagnesiumHCID 5462224—
Edukt5,6-dihydro-5-methyl-6-oxo-4H-imidazo [1,5-a]-pyrido [3,4-f][1,4]-diazepine-3-carboxaldehydeHCID 53687171—
EduktHCID 178418630HCID 178418630—
LösungsmittelHexamethylphosphoramideHCID 12679—
ProduktPyrido-[3,4-f][1,4]-diazepin-3-yl cyclopropyl carbinolHCID 137226500—

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05247079
Quelldatensatzuspto-grants-1993_09
ORD IDord-5d6c2380db7048b1ba438d1bba8589f6
Quellennotizuspto-grants-1993_09