Reaktionsgleichung
C1(=O)N(CS(Cl)(=O)=O)C(=O)C2=CC=CC=C12.C1(=O)N(CCS(Cl)(=O)=O)C(=O)C2=CC=CC=C12.C(NS(CN1C(=O)C2=CC=CC=C2C1=O)(=O)=O)(C)(C)C.C([NH:58][S:59]([CH2:62][N:63]1[C:67]([SH:68])=[N:66][N:65]=[N:64]1)(=[O:61])=[O:60])(C)(C)C.FC(F)(F)C(O)=O>>[S:59]([CH2:62][N:63]1[C:67]([SH:68])=[N:66][N:65]=[N:64]1)(=[O:61])(=[O:60])[NH2:58]Komponenten
6
Edukt 5
Produkt 1
Versuchsvorschrift
When phthalimidomethanesulfonyl chloride is substituted in the procedure of Example 3 for 2-phthalimidoethanesulfonyl chloride, N-t-butylphthalimidomethanesulfonamide is prepared which is converted to 1-N-t-butylsulfamoylmethyltetrazole-5-thiol as described therein. Treatment of 1-N-t-butylsulfamoylmethyltetrazole-5-thiol with trifluoroacetic acid as described in Example 3 gives 1-sulfamoylmethyltetrazole-5-thiol.
Aufarbeitung
- customis prepared which
Quellen und Nachweise
- ORD-Eintrag
- ord-6a12ee21dcfd4585947ce72ceeb97512
- Quelldatensatz
- uspto-grants-1979_02
- Patentnummer
- US04139701
Verknüpfte Notizen
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