Reaktion #1591318

Reaktionsgleichung

1-Ethyl-3,3,5-trimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepine-7-carbaldehyde

(2-pyridine 3-ylethyl)pyridin-4-ylmethylamine

hydrogen chloride ethyl acetate

Sodium triacetoxyborohydride

→

title compound

1-ethyl-3,3,5-trimethyl-7-{[N-(2-pyridin-3-ylethyl)-N-(pyridin-4-ylmethyl)amino]methyl}-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione trihydrochloride

Lösungsmittel

1,2-dichloroethane

acetic acid

ethyl acetate

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe mixture was stirred at room temperature overnight
2. 2
   Sonstigecondensed under reduced pressure
3. 3
   SonstigeThe residue was purified by silica gel column chromatography (ethyl acetate: methanol=100:0→90:10)
4. 4
   Sonstigecondensed under reduced pressure
5. 5
   workup.STIRRINGthe liquid was stirred at room temperature
6. 6
   SonstigeThe precipitated insoluble matter was separated
7. 7
   Waschenwashed with ethyl acetate
8. 8
   Sonstigedried

Vorschrift

1-Ethyl-3,3,5-trimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepine-7-carbaldehyde(0.92 g) and acetic acid(0.1 ml) were added to a 1,2-dichloroethane solution (15 ml) of (2-pyridine 3-ylethyl)pyridin-4-ylmethylamine(0.81 g), and the mixture was stirred for 30 minutes at room temperature. Sodium triacetoxyborohydride(0.90 g) was added, and the mixture was stirred at room temperature overnight. The reaction mixture was condensed under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate: methanol=100:0→90:10). The purified product was condensed under reduced pressure. A 4N-hydrogen chloride ethyl acetate solution(1.0 ml) was added to an ethyl acetate solution (20 ml) of the residue, and the liquid was stirred at room temperature. The precipitated insoluble matter was separated, washed with ethyl acetate, and dried to give the title compound(0.83 g) as a white solid

Quelle