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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276553Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/276553

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Methyl-4-nitrophenyl isothiocyanateHCID 145621—
Edukt1-(Chloromethyl)cyclopentan-1-amine hydrochlorideHCID 69992485—
Produkt2-(2-Methyl-4-nitrophenylimino)-3-thia-1-azaspiro[4.4]nonaneHCID 178428736—

Reaktionsschritte

1-Amino-1-(hydroxymethyl)cyclopentane was synthesized as described in Method B1c. The 2-hydroxyethylamine was reacted with SOCl2 according to Method B7a to give 1-amino-1-(chloromethyl)cyclopentane HCl salt. The 2-chloroethylamine was reacted with 2-methyl-4-nitrophenyl isothiocyanate according to Method C1e to give 2-(2-methyl-4-nitrophenylimino)-3-thia-1-azaspiro[4.4]nonane. The thiazolidine was reacted with isobutyl bromide according to Method D2a to afford 1-isobutyl-2-(2-methyl-4-nitrophenylimino)-3-thia-1-azaspiro[4.4]nonane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353006B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-e26c643647ef4bf0a71ddaa7db473c7a
Quellennotizuspto-grants-2002_03