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HRID 727243Erstellt: 24. Oktober 2026

Methyl iodide → 11H-Dibenzo(b,e)(1,4)diazepin-11-one, 5,10-dihydro-10-methyl-

https://huagongshe.com/de/reaction/727243

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
Edukt5,10-Dihydro-11H-dibenzo(b,e)(1,4)diazepin-11-oneHCID 201327—
LösungsmittelDimethylformamideHCID 6228—
Produkt11H-Dibenzo(b,e)(1,4)diazepin-11-one, 5,10-dihydro-10-methyl-HCID 3604263%

Reaktionsschritte

To a solution of 11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepine (10 g, 0.048 mol, Synthesis, (1985), 550) in dry dimethylformamide (100 ml) kept under an atmosphere of nitrogen, sodium hydride (2.1 g, 0.052 mol, 60% dispersion in oil) was added, and the reaction mixture was stirred for 1.5 h. Iodomethane (3.27 ml, 0.052 mol) was slowly added keeping the temperature below 30° C. and the mixture was stirred overnight. The reaction mixture was quenched with saturated ammonium chloride (20 ml) and poured onto ice water (300 ml). The solid was filtered off and washed with plenty of water and dried. This yielded 10.4 g of crude 10-methyl-11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepine which was recrystallised from methanol (200 ml), to give 6.7 g (63%) of 10-methyl-11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepine. M.p. 210°-211° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05712292
Quelldatensatzuspto-grants-1998_01
ORD IDord-83ecdd1848e440c79cb7d392ef7810cf
Quellennotizuspto-grants-1998_01