Bromocycloheptane → 2-(2-Methyl-4-nitrophenylimino)-1-cycloheptyl-3-thia-1-azaspiro[4.4]nonane

Beteiligte Stoffe

Reaktionsschritte

1-Hydroxymethylcyclopentanamine was prepared according to Method B1c. The 2-hydroxyethylamine was sequentially reacted with SOCl2 and 2-methyl-4-nitrophenyl isothiocyanate according to Method C2a to give 2-(2-methyl-4-nitrophenylimino)-3-thia-1-azaspiro[4.4]nonane. The thiazolidine was reacted with cycloheptyl bromide according to Method D2e to give 2-(2-methyl-4-nitrophenylimino)-1-cycloheptyl-3-thia-1-azaspiro [4.4]nonane.

Herkunft & Nachweise