1h-Pyrrolo[2,3-c]pyridine-2-methanol,a-2-pyridinyl- → (pyridin-2-yl)(1H-pyrrolo[2,3-c]pyridin-2-yl)methanone

HRID 1821897Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1821897
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH:7]([C:9]1[NH:17][C:12]2=[CH:13][N:14]=[CH:15][CH:16]=[C:11]2[CH:10]=1)[OH:8]>O1CCCC1.[O-2].[O-2].[Mn+4]>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]([C:9]1[NH:17][C:12]2=[CH:13][N:14]=[CH:15][CH:16]=[C:11]2[CH:10]=1)=[O:8]

Komponenten

4

Edukt 1

HCID 578934801h-Pyrrolo[2,3-c]pyridine-2-methanol,a-2-pyridinyl-

Produkt 1

HCID 57893522(pyridin-2-yl)(1H-pyrrolo[2,3-c]pyridin-2-yl)methanoneAusbeute 112 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 178418406HCID 178418406, VerbindungKatalysatorHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

(Pyridin-2-yl)(1H-pyrrolo[2,3-c]pyridin-2-yl)methanol (Example 117) (55 mg, 0.24 mmol) was dissolved in tetrahydrofuran (4 mL). Manganese dioxide (210 mg, 2.42 mmol) was added and the reaction mixture was stirred at room temperature for 2 h. The reaction mixture was filtered through diatomaceous earth and the filter cake was washed thoroughly with tetrahydrofuran. The organic filtrate was concentrated to a yellow solid. Drying under vacuum at 40° C. produced (pyridin-2-yl)(1H-pyrrolo[2,3-c]pyridin-2-yl)methanone (60 mg, quant.): mp 219-222° C.; 1H NMR (500 MHz, CD3OD) δ7.66-7.76 (2H, m), 7.85 (1H, m), 8.04-8.08 (1H, m), 8.14-8.21 (2H, m), 8.82-8.43 (1H, m), 8.92 (1H, s); ESI MS m/z=224 [C13H9N30+H]+; HPLC (Method A) 95.4% (AUC), tR=13.1 min.

Aufarbeitung

  1. filtrationThe reaction mixture was filtered through diatomaceous earth
  2. washthe filter cake was washed thoroughly with tetrahydrofuran
  3. concentrationThe organic filtrate was concentrated to a yellow solid
  4. customDrying under vacuum at 40° C.

Quellen und Nachweise

ORD-Eintrag
ord-fde5535486084025993c3a6bb85d0de6
Quelldatensatz
uspto-grants-2009_10
Patentnummer
US07608627B2

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