Ammonia → HCID 67370525, Verbindung

HRID 1910958Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1910958
[N:1]([C:4]1[CH:5]=[C:6]2[C:11](=[O:12])[N:10]3[CH2:13][CH2:14][N:15]([C:16]([C:18]4[C:19]([CH3:23])=[N:20][O:21][CH:22]=4)=[O:17])[C:9]3([C:24]3[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[CH:26][CH:25]=3)[CH2:8][N:7]2[CH:32]=1)=[N+:2]=[N-:3].[C:33]([Si:35]([CH3:38])([CH3:37])[CH3:36])#[CH:34].C(N(C(C)C)C(C)C)C.[NH4+].[Cl-].N>CN(C=O)C.[Cu](I)I>[CH3:31][O:30][C:27]1[CH:28]=[CH:29][C:24]([C:9]23[N:15]([C:16]([C:18]4[C:19]([CH3:23])=[N:20][O:21][CH:22]=4)=[O:17])[CH2:14][CH2:13][N:10]2[C:11](=[O:12])[C:6]2[N:7]([CH:32]=[C:4]([N:1]4[CH:34]=[C:33]([Si:35]([CH3:38])([CH3:37])[CH3:36])[N:3]=[N:2]4)[CH:5]=2)[CH2:8]3)=[CH:25][CH:26]=1

Komponenten

8

Edukt 5

HCID 222AmmoniaHCID 25517Ammonium ChlorideHCID 66111TrimethylsilylacetyleneHCID 81531DiisopropylethylamineHCID 86657086HCID 86657086, Verbindung

Produkt 1

HCID 67370525HCID 67370525, VerbindungAusbeute 23 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 83717Copper iodideKatalysatorHCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of 7-azido-10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one (50 mg, 0.116 mmol) in DMF (2.5 mL) at 0° C. was added ethynyl-trimethyl-silane (33 μL, 0.23 mmol) followed by ethyl-diisopropyl-amine (24 μL, 0.14 mmol) and copper iodide (11 mg) and the mixture was stirred at 0° C. After one hour the reaction was complete (monitored by LCMS). A saturated aqueous solution of NH4Cl containing a drop of ammonia was added and the mixture extracted with EtOAc (3 times). The organics were washed with brine, dried (Na2SO4), filtrated and concentrated in vacuo. The resulting material was purified by flash chromatography (Biotage SP4, gradient 50-100% EtOAc in hexanes 10 CV; hold 100% EtOAc 7CV) to give 10a-(4-methoxyphenyl)-1-[(3-methyl-1,2-oxazol-4-yl)carbonyl]-7-[4-(trimethylsilyl)-1H-1,2,3-triazol-1-yl]-2,3,10,10a-tetrahydro-1H,5H-imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one (14 mg, yield: 23%). ESI-MI m/z [M+H]+ 532.2.

Aufarbeitung

  1. extractionthe mixture extracted with EtOAc (3 times)
  2. washThe organics were washed with brine
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltrated
  5. concentrationconcentrated in vacuo
  6. customThe resulting material was purified by flash chromatography (Biotage SP4, gradient 50-100% EtOAc in hexanes 10 CV; hold 100% EtOAc 7CV)

Quellen und Nachweise

ORD-Eintrag
ord-ec0f2ad2787b4074bd214a3a752d5a89
Quelldatensatz
uspto-grants-2013_12
Patentnummer
US08604034B2

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