Sodium Azide → HCID 178440795, Verbindung
Reaktionsgleichung
[Cl-].[Al+3].[Cl-].[Cl-].[N-:5]=[N+:6]=[N-:7].[Na+].[C:9]1([C:15]([C:25]2[CH:30]=[CH:29][C:28]([CH:31]=[CH:32][C:33]#[N:34])=[CH:27][CH:26]=2)=[C:16]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:17][CH3:18])[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>C1COCC1.Cl>[C:9]1([C:15]([C:25]2[CH:30]=[CH:29][C:28]([CH:31]=[CH:32][C:33]3[NH:34][N:7]=[N:6][N:5]=3)=[CH:27][CH:26]=2)=[C:16]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:17][CH3:18])[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a solution of aluminum chloride (1.82 g, 13.5 mmol) in THF (20 mL) at 0° C. was added sodium azide (1.77 g, 27 mmol) then nitrile (4b) (888 mg, 2.65 mmol). The mixture was stirred 10 min and heated to reflux. After refluxing overnight the mixture was diluted with 1N HCl, and extracted with EtOAc. The combined organic layers were washed with water, brine and dried (MgSO4). The solvent was removed under reduced pressure and the residue chromatographed (silica gel, 10-20% methanol/CH2Cl2) to give the tetrazole (4c) as a white solid (700 mg, 70%): 1H NMR (CDCl3) δ 7.63 (d, J=16.5 Hz, 1H), 7.39-7.11 (m, 12H), 6.98 (d, J=16.5 Hz, 1H), 6.91 (d, J=8.4 Hz, 2H), 2.48 (q, J=7.3 Hz, 2H), 0.94 (t, J=7.3 Hz, 3H); ESI m/z: 377 (M−H−, 100%).
Aufarbeitung
- temperatureheated to reflux
- temperatureAfter refluxing overnight the mixture
- extractionextracted with EtOAc
- washThe combined organic layers were washed with water, brine
- dry with materialdried (MgSO4)
- customThe solvent was removed under reduced pressure
- customthe residue chromatographed (silica gel, 10-20% methanol/CH2Cl2)
Quellen und Nachweise
- ORD-Eintrag
- ord-bd3592927b8746a1a39fcececabd58c2
- Quelldatensatz
- uspto-grants-2008_01
- Patentnummer
- US07323587B2
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