Reaktion #77568

ord-b7d77866183941db9012d90e0a4e417a

Reaktionsgleichung

Brc1ccc(N2CCCN(c3ccc(Br)cn3)CC2)nc1
1,4-bis(5-bromo-2-pyridyl)hexahydro-1,4-diazepine
Cc1ccc(B(O)O)cc1
4-methylphenylboronic acid
Cc1ccc(-c2ccc(N3CCCN(c4ccc(-c5ccc(C)cc5)cn4)CC3)nc2)cc1
title compound
Ausbeute 42.8%
Cc1ccc(-c2ccc(N3CCCN(c4ccc(-c5ccc(C)cc5)cn4)CC3)nc2)cc1
1,4-Bis[5-(4-methylphenyl)-2-pyridyl]hexahydro-1,4-diazepine
Ausbeute 42.8%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe crude crystals were recrystallized from chloroform-hexane

Vorschrift

Following the procedure of Example 1, crude crystals were obtained from the 1,4-bis(5-bromo-2-pyridyl)hexahydro-1,4-diazepine (206.0 mg, 0.500 mmol) synthesized in Reference Example 1 and 4-methylphenylboronic acid (163.0 mg, 1.20 mmol). The crude crystals were recrystallized from chloroform-hexane to yield the title compound as pale yellow needles (melting point: 245.0-247.0° C.)(93.0 mg, yield: 42%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06706703B2uspto-grants-2004_03