Ethanol → 4'-({4-[4-(2-Hydroxyethylidene)cyclohexyl]-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile

HRID 519575Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 519575
[Cl-].[Ca+2].[Cl-].[BH4-].[Na+].C(O)C.[C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[C:17]1[CH:22]=[CH:21][C:20]([CH2:23][C:24]2[C:25](=[O:48])[N:26]([CH:36]3[CH2:41][CH2:40][C:39](=[CH:42][C:43](OCC)=[O:44])[CH2:38][CH2:37]3)[C:27]3[N:28]([N:33]=[CH:34][N:35]=3)[C:29]=2[CH2:30][CH2:31][CH3:32])=[CH:19][CH:18]=1)#[N:10]>O1CCCC1>[OH:44][CH2:43][CH:42]=[C:39]1[CH2:40][CH2:41][CH:36]([N:26]2[C:25](=[O:48])[C:24]([CH2:23][C:20]3[CH:21]=[CH:22][C:17]([C:12]4[C:11]([C:9]#[N:10])=[CH:16][CH:15]=[CH:14][CH:13]=4)=[CH:18][CH:19]=3)=[C:29]([CH2:30][CH2:31][CH3:32])[N:28]3[N:33]=[CH:34][N:35]=[C:27]23)[CH2:37][CH2:38]1

Komponenten

6

Edukt 4

HCID 702EthanolHCID 4311764Sodium borohydrideHCID 5284359Calcium ChlorideHCID 86644029ethyl (4-{6-[(2'-cyanobiphenyl-4-yl)methyl]-5-oxo-7-propyl[1,2,4]triazolo[1,5-a]pyrimidin-4(5H)-yl}cyclohexylidene)acetate

Produkt 1

HCID 670092204'-({4-[4-(2-Hydroxyethylidene)cyclohexyl]-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrileAusbeute 51,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A mixture of calcium chloride (1.6 g), sodium borohydride (1.1 g), tetrahydrofuran (40 mL) and ethanol (40 mL) was stirred at 0° C. for 1 hr. A solution (20 mL) of ethyl (4-{6-[(2′-cyanobiphenyl-4-yl)methyl]-5-oxo-7-propyl[1,2,4]triazolo[1,5-a]pyrimidin-4(5H)-yl}cyclohexylidene)acetate (1.9 g) in tetrahydrofuran was added to the reaction mixture, and the mixture was stirred at room temperature for 16 hr. The reaction mixture was extracted with 1 N hydrochloric acid and ethyl acetate, and the obtained ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.9 g, 49%).

Aufarbeitung

  1. stirringthe mixture was stirred at room temperature for 16 hr
  2. extractionThe reaction mixture was extracted with 1 N hydrochloric acid and ethyl acetate
  3. washthe obtained ethyl acetate layer was washed with saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customThe solvent was evaporated under reduced pressure
  6. customthe residue was purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-a2f42cae5e2747c0ba54bb1a82243774
Quelldatensatz
uspto-grants-2015_08
Patentnummer
US09115136B2

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