Aluminium lithium hydride → 2-[1-Benzyl-3-(4-chloro-phenyl)-4,5,7,8-tetrahydro-1H-1,2,6-triaza-azulen-6-yl]-ethanol

HRID 2106287Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2106287
C[O:2][C:3](=O)[CH2:4][N:5]1[CH2:14][CH2:13][C:12]2[N:11]([CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[N:10]=[C:9]([C:22]3[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][CH:23]=3)[C:8]=2[CH2:7][CH2:6]1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[CH2:15]([N:11]1[C:12]2[CH2:13][CH2:14][N:5]([CH2:4][CH2:3][OH:2])[CH2:6][CH2:7][C:8]=2[C:9]([C:22]2[CH:27]=[CH:26][C:25]([Cl:28])=[CH:24][CH:23]=2)=[N:10]1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

Komponenten

4

Versuchsvorschrift

To a solution of [1-benzyl-3-(4-chloro-phenyl)-4,5,7,8-tetrahydro-1H-1,2,6-triaza-azulen-6-yl]-acetic acid methyl ester (Example 170, 16 mg) in THF (1 mL) was added lithium aluminum hydride (100 mg). The mixture was stirred at RT for 16 h. The reaction was quenched by the addition of H2O (0.1 mL). Concentration and purification (SiO2, 2 M NH3 in MeOH/CH2Cl2) provided the title compound (5 mg). MS (ESI): exact mass calculated for C22H24ClN3O, 381.16; found, m/z 382.1 [M+H]+. 1H NMR (500 MHz, CDCl3): 7.50-7.20 (m, 7H), 7.04 (d, J=7.2 Hz, 1H), 5.29 (s, 2H), 3.07-3.04 (m, 2H), 2.89-2.77 (m, 10H).

Aufarbeitung

  1. customThe reaction was quenched by the addition of H2O (0.1 mL)
  2. concentrationConcentration and purification (SiO2, 2 M NH3 in MeOH/CH2Cl2)

Quellen und Nachweise

ORD-Eintrag
ord-5c5e1a2dcc0c4cd6902d8166459b3b7c
Quelldatensatz
uspto-grants-2009_08
Patentnummer
US07579470B2

Notizen zur Reaktion

Wird geladen…