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HRID 25059Erstellt: 26. Oktober 2026

Potassium Chloride → (+/-)-8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine-7-carbonitrile

https://huagongshe.com/reaction/25059

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium ChlorideHCID 4873—
EduktDimethylformamideHCID 6228—
EduktCyanogen BromideHCID 10476—
Edukt1-(4-Nitrophenyl)-4-methyl-7,8-methylenedioxy-3,4-dihydro-5H-2,3-benzodiazepineHCID 10336422—
LösungsmittelWaterHCID 962—
Produkt(+/-)-8-Methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine-7-carbonitrileHCID 1213741695%

Reaktionsschritte

A mixture of 3.25 g (10 mmol) of (±)-8-methyl-5-(4-nitrophenyl)-8,9-dihydro-7H-1,3-dioxolo[4,5-h][2,3]benzodiazepine, 20 ml of dimethylformamide, 2.76 g (20 mmol) of potassium chloride and 1.80 g (17 mmol) of cyanogen bromide was stirred at room temperature for 20 h. After pouring into water, the precipitated crystals were filtered off, and washed with water to yield 3.34 g (95%) of the title compound, Mp.: 172-176° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858605B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-fc559d231c654a62a357da91edbcf1d0
Quellennotizuspto-grants-2005_02