Reaktionsgleichung
I[CH2:2][CH:3]1[S:7][CH2:6][CH:5]([S:8][C:9](=[O:11])[CH3:10])[CH2:4]1.[N-:12]=[N+:13]=[N-:14].C([N+](CCCC)(CCCC)CCCC)CCC>C(Cl)Cl>[N:12]([CH2:2][CH:3]1[S:7][CH2:6][CH:5]([S:8][C:9](=[O:11])[CH3:10])[CH2:4]1)=[N+:13]=[N-:14]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution, under argon, of 0.183 g of product from Example 140 in 1.0 ml of dry methylene chloride is treated with 0.689 g of tetra-n-butyl-ammonium azide. The reaction mixture is stirred vigorously overnight at room temperature. The reaction is concentrated in vacuo and the residue purified by chromatography (silica gel: 0-10% diethyl ether/hexane) to give 0.061 g of the desired product.
Aufarbeitung
- concentrationThe reaction is concentrated in vacuo
- customthe residue purified by chromatography (silica gel: 0-10% diethyl ether/hexane)
Quellen und Nachweise
- ORD-Eintrag
- ord-898193f0f65f4694bd51481f91ebc822
- Quelldatensatz
- uspto-grants-1997_04
- Patentnummer
- US05623081
Verknüpfte Notizen
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