反応 #2040064

ord-93a8498e5bb643bd8955f35b45abfa41

反応方程式

O=C(O)c1cccc2cc3ccccc3nc12.c1c[n-]cn1
acridine-4-carboxylic acid imidazolide
NCCCNCCCN
N,N-bis(3-aminopropyl)amine
O=C(NCCCNCCCNC(=O)c1cccc2cc3ccccc3nc12)c1cccc2cc3ccccc3nc12
bis[3-(acridine-4-carboxamido)propyl]amine
収率 80.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他followed by purification of the product by chromatography on alumina-90
  2. 2
    洗浄eluting with CH2Cl2 /MeOH (20:1)

実験手順

Similar reaction of acridine-4-carboxylic acid imidazolide with N,N-bis(3-aminopropyl)amine as above, followed by purification of the product by chromatography on alumina-90, eluting with CH2Cl2 /MeOH (20:1), gave bis[3-(acridine-4-carboxamido)propyl]amine (35) (80%) as an oil. 1H NMR [(CD3)2SO] δ 11.40 (t, J=5.4 Hz, 2 H, 2×CONH), 9.19 (s, 2 H, H-9), 8.71 (d, J=7.1 Hz, 2 H, H-3), 8.32 (d, J=8.5 Hz, 2 H, ArH), 8.18-8.00 (m, 4 H, ArH), 7.83-7.62 (m, 4 H, ArH), 7.51 (t, J=7.5 Hz, 2H, ArH), 3.64 (q, J=6.0 Hz, 4H, 2×CONHCH2) 2.86 (t, J=6.7 Hz, 4H, CH2NHCH2) 1.92 (quint, J=6.5 Hz, 4 H, 2×CH2CH2CH2). Crystallization from MeOH/EtOAc/HCl gave the trihydrochloride salt, mp 171-173° C. Anal. (C34H31N5O2.2HCl.2H2O) C, H, N, Cl.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06114332uspto-grants-2000_09