Acetic Acid → HCID 57495630, Verbindung

HRID 1092345Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1092345
Cl.[NH2:2][CH:3]1[CH:10]2[CH2:11][C:6]3([OH:14])[CH2:7][C:8]([OH:13])([CH2:12][CH:4]1[CH2:5]3)[CH2:9]2.[C:15]([NH:22][C:23]1([CH:28]=O)[CH2:27][CH2:26][CH2:25][CH2:24]1)([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16].C(O)(=O)C.C([O-])(O)=O.[Na+]>CO.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>[C:18]([O:17][C:15](=[O:16])[NH:22][C:23]1([CH2:28][NH:2][CH:3]2[CH:10]3[CH2:9][C:8]4([OH:13])[CH2:7][C:6]([OH:14])([CH2:5][CH:4]2[CH2:12]4)[CH2:11]3)[CH2:24][CH2:25][CH2:26][CH2:27]1)([CH3:21])([CH3:19])[CH3:20]

Komponenten

7

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a mixture of 6-amino-adamantane-1,3-diol hydrochloride (258 mg, J. Med. Chem. 50, 2007, 149), N-Boc-cycloleucinal (250 mg) and acetic acid (0.67 ml) in MeOH (5.0 ml), sodium triacetoxyborohydride was added at room temperature. The mixture was stirred at 60° C. for 30 min. The mixture was basified with saturated NaHCO3 solution. The mixture was extracted with AcOEt, washed with brine, dried over MgSO4 and evaporated. The residue was purified with silica gel chromatography (CH2Cl2:MeOH:NH4OH=from 100:0:0 to 90:9:1) to obtain the title compound (250 mg, 56%) as a white amorphous.

Aufarbeitung

  1. additionwas added at room temperature
  2. extractionThe mixture was extracted with AcOEt
  3. washwashed with brine
  4. dry with materialdried over MgSO4
  5. customevaporated
  6. customThe residue was purified with silica gel chromatography (CH2Cl2:MeOH:NH4OH=from 100:0:0 to 90:9:1)

Quellen und Nachweise

ORD-Eintrag
ord-3f6498360f464d6caefacd9f6a365a9a
Quelldatensatz
uspto-grants-2012_03
Patentnummer
US08129423B2

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