Реакция #58074

ord-444d699f6dbe4e46b2d0546ca48611c4

Уравнение реакции

[N-]=[N+]=NC(=O)CC1=CCNC(=O)c2[nH]c3ccc(F)cc3c21
(7-Fluoro-1-oxo-1,2,3,10-tetrahydro-azepino[3,4-b]indol-5-yl)-acetyl azide
CN(C)CCN
N,N-dimethylethylene-diamine
CN(C)CCNC(=O)C=C1CCNC(=O)c2[nH]c3ccc(F)cc3c21
N-(2-dimethylamino-ethyl)-2-(7-fluoro-1-oxo-1,3,4,10-tetrahydro-2H-azepino[3,4-b]indol-5-ylidene)-acetamide

Растворители

Условия реакции

Температура
110°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеToluene is removed in vacuum
  2. 2
    Другоеthe residue is purified by HPLC (C18 column, eluted with CH3CN/H2O with 0.5% TFA)

Методика

A suspension of (7-Fluoro-1-oxo-1,2,3,10-tetrahydro-azepino[3,4-b]indol-5-yl)-acetyl azide, prepared as in reference 17, (10 mg, 0.33 mmol) and N,N-dimethylethylene-diamine (15 mg, 0.17 mmol) in dry toluene (1 mL) is heated at 110° C. for 1 hour. Toluene is removed in vacuum and the residue is purified by HPLC (C18 column, eluted with CH3CN/H2O with 0.5% TFA) to afford N-(2-dimethylamino-ethyl)-2-(7-fluoro-1-oxo-1,3,4,10-tetrahydro-2H-azepino[3,4-b]indol-5-ylidene)-acetamide; 1H NMR (DMSO-d6) δ 2.85 (s, 6H), 3.19-3.22 (m, 2H), 3.25-3.30 (m, 2H), 3.44-3.48 (m, 2H), 3.49 (q, 2H, J=6.8 Hz), 6.34 (s, 1H), 7.18 (dt, 1H, J1=2.8 Hz, J2=8.8 Hz), 7.50 (dd, 1H, J1=4.4 Hz, J2=8.8 Hz), 7.74 (dd, 1H, J1=2.8 Hz, J2=10.4 Hz), 8.39-8.44 (m, 2H), 9.36 (bs, 1H), 12.12 (s, 1H); m/z [M++1] 345.1.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07423031B2uspto-grants-2008_09