Benzyl azide → HCID 68990558, Verbindung
Reaktionsgleichung
[CH2:1]([N:4]1[C:8](=[O:9])[C:7]2=[CH:10][CH:11]=[CH:12][CH:13]=[C:6]2[C:5]1=[O:14])[C:2]#[CH:3].[CH2:15]([Sn:19]([CH2:27][CH2:28][CH2:29][CH3:30])([CH2:23][CH2:24][CH2:25][CH3:26])N(C)C)[CH2:16][CH2:17][CH3:18].[CH2:31]([N:38]=[N+:39]=[N-:40])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>CCCCCC>[CH2:31]([N:38]1[C:2]([CH2:1][N:4]2[C:8](=[O:9])[C:7]3[C:6](=[CH:13][CH:12]=[CH:11][CH:10]=3)[C:5]2=[O:14])=[C:3]([Sn:19]([CH2:15][CH2:16][CH2:17][CH3:18])([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:27][CH2:28][CH2:29][CH3:30])[N:40]=[N:39]1)[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 70 °C
Versuchsvorschrift
N-Propargylphthalimide (2.35 g mg, 12.7 mmol) was added to 1,1,1-tributyl-N,N-dimethylstannanamine (4.23 mg, 12.7 mmol) in hexane (3.0 mL) and stirred in a sealed vial at 70° C. for 2 hours. The mixture was cooled to ambient temperature and the vial was stirred unsealed for 10 minutes. Benzyl azide (2.0 mL, 16.0 mmol) was added and the vial was resealed and heated to 130° C. overnight. The mixture was purified by silica gel chromatography eluting with a gradient of 10-50% ethyl acetate in hexanes to afford the title compound. MS (ESI+) m/z 609.3 (M+H)+.
Aufarbeitung
- temperatureThe mixture was cooled to ambient temperature
- stirringthe vial was stirred unsealed for 10 minutes
- temperatureheated to 130° C. overnight
- customThe mixture was purified by silica gel chromatography
- washeluting with a gradient of 10-50% ethyl acetate in hexanes
Quellen und Nachweise
- ORD-Eintrag
- ord-4e672f7ca4f141aea9d65471bf205c1e
- Quelldatensatz
- uspto-grants-2014_02
- Patentnummer
- US08648069B2
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