Sodium Cyanide → 1-(4-(Pyridin-4-yloxy)phenylamino)-cyclobutanecarbonitrile
Reaktionsgleichung
[C-:1]#[N:2].[Na+].[N:4]1[CH:9]=[CH:8][C:7]([O:10][C:11]2[CH:17]=[CH:16][C:14]([NH2:15])=[CH:13][CH:12]=2)=[CH:6][CH:5]=1.[C:18]1(=O)[CH2:21][CH2:20][CH2:19]1>CC(O)=O>[N:4]1[CH:5]=[CH:6][C:7]([O:10][C:11]2[CH:17]=[CH:16][C:14]([NH:15][C:18]3([C:1]#[N:2])[CH2:21][CH2:20][CH2:19]3)=[CH:13][CH:12]=2)=[CH:8][CH:9]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Sodium cyanide (395 mg, 8.06 mmol) was added to a mixture of 4-(pyridin-4-yloxy)aniline (500 mg, 2.69 mmol) and cyclobutanone (376 mg, 5.37 mmol) in AcOH (99%, 6 mL) in a microwave vial. The reaction mixture was irradiated with microwaves (Biotage) at 120° C. for 30 min. The slightly yellowish solution was concentrated to dryness. The residue was diluted with water and extracted with EtOAc (2×). The combined organic layers were dried over MgSO4 and concentrated to dryness to afford 463 mg (65%) of 1-(4-(pyridin-4-yloxy)phenylamino)-cyclobutanecarbonitrile as a yellow oil. 1H NMR (400 MHz, CDCl3) δ 8.46-8.38 (m, 2H), 7.02-6.94 (m, 2H), 6.79 (m, 2H), 6.72-6.64 (m, 2H), 2.86-2.74 (m, 2H), 2.46-2.34 (m, 2H), 2.22 (m, 2H)
Aufarbeitung
- customThe reaction mixture was irradiated with microwaves (Biotage) at 120° C. for 30 min
- concentrationThe slightly yellowish solution was concentrated to dryness
- additionThe residue was diluted with water
- extractionextracted with EtOAc (2×)
- dry with materialThe combined organic layers were dried over MgSO4
- concentrationconcentrated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-7b408df272a0413aab6bd93323467c4f
- Quelldatensatz
- uspto-grants-2015_08
- Patentnummer
- US09108944B2
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