Ethyl Acetate → Ethyl 4-hydroxymethyl-2-propyl-{4-[2-(trityltetrazol-5-yl)phenyl]phenyl}methylimidazole-5-carboxylate

HRID 265049Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 265049
[H-].C([Al+]CC(C)C)C(C)C.[CH2:11]([C:14]1[N:15]([CH2:29][C:30]2[CH:35]=[CH:34][C:33]([C:36]3[CH:41]=[CH:40][CH:39]=[CH:38][C:37]=3[C:42]3[N:46]([C:47]([C:60]4[CH:65]=[CH:64][CH:63]=[CH:62][CH:61]=4)([C:54]4[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=4)[C:48]4[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=4)[N:45]=[N:44][N:43]=3)=[CH:32][CH:31]=2)[C:16]([C:24]([O:26][CH2:27][CH3:28])=[O:25])=[C:17]([C:19](OCC)=[O:20])[N:18]=1)[CH2:12][CH3:13].C(OCC)(=O)C.[Cl-].[NH4+]>C1(C)C=CC=CC=1.O1CCCC1>[OH:20][CH2:19][C:17]1[N:18]=[C:14]([CH2:11][CH2:12][CH3:13])[N:15]([CH2:29][C:30]2[CH:31]=[CH:32][C:33]([C:36]3[CH:41]=[CH:40][CH:39]=[CH:38][C:37]=3[C:42]3[N:46]([C:47]([C:54]4[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=4)([C:48]4[CH:49]=[CH:50][CH:51]=[CH:52][CH:53]=4)[C:60]4[CH:61]=[CH:62][CH:63]=[CH:64][CH:65]=4)[N:45]=[N:44][N:43]=3)=[CH:34][CH:35]=2)[C:16]=1[C:24]([O:26][CH2:27][CH3:28])=[O:25]

Komponenten

7

Edukt 4

HCID 8857Ethyl AcetateHCID 25517Ammonium ChlorideHCID 19036089Diethyl 2-propyl-1-((2'-(1-trityl-1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-imidazole-4,5-dicarboxylateHCID 21225700Diisobutylaluminumhydride

Produkt 1

HCID 19036205Ethyl 4-hydroxymethyl-2-propyl-{4-[2-(trityltetrazol-5-yl)phenyl]phenyl}methylimidazole-5-carboxylateAusbeute 100,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1140TolueneLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

10 ml of a 1.5M solution of diisobutylaluminum hydride in toluene were added dropwise at -20° C. under an atmosphere of nitrogen to a solution of 4.27 g of diethyl 2-propyl-1-{4-[2-(trityltetrazol-5-yl)phenyl]phenyl}methylimidazole-4,5-dicarboxylate [prepared as described in step (a) above] in 50 ml of tetrahydrofuran. The resulting mixture was allowed to stand at 0° C. for 16 hours and then mixed with ethyl acetate and with a saturated aqueous solution of ammonium chloride; it was then stirred at room temperature for 1 hour. The resulting precipitate was filtered off, and the ethyl acetate layer was separated and dried over anhydrous magnesium sulfate; the solvent was then removed by distillation under reduced pressure. The crystalline residue was washed with diisopropyl ether, to give 4.03 g of the title compound, melting at 135°-138° C.

Aufarbeitung

  1. filtrationThe resulting precipitate was filtered off
  2. customthe ethyl acetate layer was separated
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customthe solvent was then removed by distillation under reduced pressure
  5. washThe crystalline residue was washed with diisopropyl ether

Quellen und Nachweise

ORD-Eintrag
ord-7f09f487e8494b70bc1ccc65188eab85
Quelldatensatz
uspto-grants-1997_07
Patentnummer
US05646171

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