Reaktion #65134

ord-79eaf72784de43c4af5c7a91e5d67ae8

Reaktionsgleichung

O=C(Cl)CCCCl
4-chlorobutyryl chloride
O=C1Nc2ccccc2Nc2ccccc21
10,11-dihydrodibenzo[b,e][1,4]diazepin-11-one
O=C1Nc2ccccc2N(C(=O)CCCCl)c2ccccc21
title compound
O=C1Nc2ccccc2N(C(=O)CCCCl)c2ccccc21
5- (4-Chlorobutyryl)-10,11-dihydrodibenzo [b,e][1,4]diazepin-11-one

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturunder reflux for 8 hours
  3. 3
    Sonstigeevaporated
  4. 4
    SonstigeThe residue was purified by chromatography on silica
  5. 5
    Sonstigeevaporated
  6. 6
    Sonstigethe residue triturated with hexane/dichloromethane

Vorschrift

A mixture of 4-chlorobutyryl chloride (3.5 g) and 10,11-dihydrodibenzo[b,e][1,4]diazepin-11-one (4.2 g) (J. Med. Chem., 1963, 6, 767) in acetone (90 ml) was heated under reflux for 8 hours and evaporated. The residue was purified by chromatography on silica using hexane plus 0-100% dichloromethane as eluant. Appropriate fractions were combined and evaporated and the residue triturated with hexane/dichloromethane to give the title compound as a colourless solid, 1.62 g (26%), m.p. 151°-152° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05418229uspto-grants-1995_05