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HRID 356144Erstellt: 25. Oktober 2026

Sodium hydride → 9-(4-Nitrobenzyl)-2,3,9,10a-tetrahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one

https://huagongshe.com/reaction/356144

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
Edukt4-Nitrobenzyl bromideHCID 66011—
Edukt2,3,9,10a-Tetrahydro-1H-benzo[b]cyclopenta[f][1,4]diazepin-10-oneHCID 12394935—
LösungsmittelDimethylformamideHCID 6228—
Produkt9-(4-Nitrobenzyl)-2,3,9,10a-tetrahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-oneHCID 7011296471%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A suspension of 2,3,9,10a-tetrahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one (25.00 g, 0.125 mol.) in N,N-dimethylformamide (150 mL) was cooled to 0° C., to which was added sodium hydride (60% liquid paraffin dispersion, 5.00 g, 0.125 mol.). This mixture was stirred for 10 minutes at the same temperature and for 5 minutes at 20° C. This solution was cooled to 0° C., to which was added 4-nitrobenzyl bromide (28.32 g, 0.131 mol.), and the mixture was stirred for 10 minutes at 20° C. The reaction mixture was poured into a saturated aqueous solution of ammonium chloride (500 mL). Resulting precipitate was subjected to filtration, and washed with water, followed by recrystallization from dichloromethane-ethanol to give 29.76 g (yield 71%) of the titled compound. The sample for analylical experiment was prepared by recrystallization of the compound from chloroform-ethanol, m.p. 185°-188° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05834463
Quelldatensatzuspto-grants-1998_11
ORD IDord-986ae27d19904754ad8ec8c82ad9b3f0
Quellennotizuspto-grants-1998_11