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Potassium Carbonate → (R)-tert-Butyl 1-methoxy-3-(3-oxo-4-(m-tolylamino)-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)propan-2-ylcarbamate

HRID 711543
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 711543
[C:1]([O:5][C:6]([NH:8][C@@H:9]([CH2:32][O:33][CH3:34])[CH2:10][NH:11][C:12]1[CH:21]=[C:20]([C:22]#[N:23])[C:15]([C:16]([O:18]C)=O)=[C:14]([NH:24][C:25]2[CH:26]=[C:27]([CH3:31])[CH:28]=[CH:29][CH:30]=2)[N:13]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+]>C(O)(=O)C.C(Cl)Cl.[Pt](=O)=O>[CH3:34][O:33][CH2:32][C@H:9]([NH:8][C:6](=[O:7])[O:5][C:1]([CH3:3])([CH3:2])[CH3:4])[CH2:10][NH:11][C:12]1[N:13]=[C:14]([NH:24][C:25]2[CH:26]=[C:27]([CH3:31])[CH:28]=[CH:29][CH:30]=2)[C:15]2[C:16](=[O:18])[NH:23][CH2:22][C:20]=2[CH:21]=1
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Komponenten

6

Edukt 2

HCID 11430Potassium CarbonateHCID 67238996(R)-Methyl 6-(2-(tert-butoxycarbonylamino)-3-methoxypropylamino)-4-cyano-2-(m-tolylamino)nicotinate

Produkt 1

HCID 67238901(R)-tert-Butyl 1-methoxy-3-(3-oxo-4-(m-tolylamino)-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)propan-2-ylcarbamate

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 345198Adams' catalystKatalysator
HCID 176
Acetic Acid
Lösungsmittel
HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a round-bottomed flask was added (R)-methyl 6-(2-(tert-butoxycarbonylamino)-3-methoxypropylamino)-4-cyano-2-(m-tolylamino)nicotinate (84.5 mg, 0.180 mmol) in acetic acid (3 mL) and DCM (10 mL). To the resulting yellow solution was added platinum(IV) oxide (4.09 mg, 0.018 mmol). The flask was evacuated and back filled with hydrogen (3×1 atm). The reaction mixture was stirred vigorously at RT for 16 h, subsequently diluted with DCM (10 mL), and filtered through Celite. The filtrate was concentrated to an oil, which was diluted with DCM (10 mL). Potassium carbonate (24.87 mg, 0.180 mmol) was added and the reaction mixture was stirred at RT for 12 h. The crude reaction was diluted with DCM (10 mL), filtered through Celite, and concentrated to give the title compound as a thick yellow oil, which was used without further purification (26.5 mg, 33.4%). [M+H] calc'd for C23H31N5O4, 442. found, 442.

Aufarbeitung

  1. customThe flask was evacuated
  2. additionback filled with hydrogen (3×1 atm)
  3. additionsubsequently diluted with DCM (10 mL)
  4. filtrationfiltered through Celite
  5. concentrationThe filtrate was concentrated to an oil, which
  6. additionwas diluted with DCM (10 mL)
  7. stirringthe reaction mixture was stirred at RT for 12 h
  8. customThe crude reaction
  9. filtrationfiltered through Celite
  10. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-74f4aac8e3134f3a82549d6965326bf3
Quelldatensatz
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09181255B2

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