Urea → 1-(2,2-Diphenyl-ethyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid amide

HRID 1071990Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1071990
[C:1]1([CH:7]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH2:8][CH:9]2[C:18]3[C:13](=[CH:14][C:15]([O:21][CH3:22])=[C:16]([O:19][CH3:20])[CH:17]=3)[CH2:12][CH2:11][NH:10]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:29][C:30](N)=[O:31]>>[C:30]([N:10]1[CH2:11][CH2:12][C:13]2[C:18](=[CH:17][C:16]([O:19][CH3:20])=[C:15]([O:21][CH3:22])[CH:14]=2)[CH:9]1[CH2:8][CH:7]([C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)(=[O:31])[NH2:29]

Komponenten

3

Versuchsvorschrift

A solution of 1-(2,2-diphenyleth-1-yl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline (1.0598 g, 2.838 mmoles) and urea (1.704 g, 10 equiv.) was heated at reflux. After 3 hours, TLC indicated less than 15% conversion. More urea (15.5 g, 90 equiv.) was added. Reflux continued for 24 hours. The solvent was then evaporated and the residue dissolved in water (80 mL). A white solid formed. After 1 hour, the solid was collected by filtration, washed with water, and dried in vacuo overnight (1.0554 g, 89%). 1H-NMR (CDCl3) δ 2.49 (m, 1H), 2.69 (m, 2H), 2.90 (m, 1H), 3.37 (m, 1H), 3.82 (s, 3H), 3.86 (s, 3H), 3.89 (m, 2H), 4.05 (t, 1H), 4.38 (m, 1H), 6.41 (s, 1H), 6.60 (s, 1H), 7.29 (m, 10H). Mass spec. 417.3 (MH)+. Anal. Calc. for C26H28N2O3: C-74.98, H-6.78, N-6.73. Found: C-74.72, H-6.74, N-6.45.

Aufarbeitung

  1. temperatureat reflux
  2. temperatureReflux
  3. waitcontinued for 24 hours
  4. customThe solvent was then evaporated
  5. dissolutionthe residue dissolved in water (80 mL)
  6. customA white solid formed
  7. waitAfter 1 hour
  8. filtrationthe solid was collected by filtration
  9. washwashed with water
  10. customdried in vacuo overnight (1.0554 g, 89%)

Quellen und Nachweise

ORD-Eintrag
ord-8ed5401d42754f188ce6e0017c1c2b7d
Quelldatensatz
uspto-grants-2005_06
Patentnummer
US06908931B2

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