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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276698Erstellt: 26. Oktober 2026

2-Chloroethylamine → 1-Cyclohexyl-2-(2-methyl-4-nitrophenylimino)-3-oxa-1-azaspiro[4.4]nonane

https://huagongshe.com/reaction/276698

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-ChloroethylamineHCID 13369—
EduktThionyl ChlorideHCID 24386—
Edukt2-Methyl-4-nitrophenyl isocyanateHCID 4296456—
Edukt1-(Cyclohexylamino)-1-(chloromethyl)cyclopentaneHCID 18316166—
Produkt1-Cyclohexyl-2-(2-methyl-4-nitrophenylimino)-3-oxa-1-azaspiro[4.4]nonaneHCID 18316338—

Reaktionsschritte

1-Aminocyclopentanecarboxylic acid was converted to the methyl ester according to Method B1c, Step 1. The ester reduced to 1-hydroxymethylcyclopentanamine according to Method B1c, Step 2. The hydroxyethylamine was reacted with cyclohexanone according to Method B4a, Step 1 to give 6-aza-13-oxadispiro[4.1.5.2]tetradecane. The oxazolidine was reduced according to Method B4a, Step 2 to give 1-(cyclohexylamino)-1-(hydroxymethyl)cyclopentane. The substituted 2-hydroxyethylamine was reacted with SOCl2 according to Method B7b to 1-(cyclohexylamino)-1-(chloromethyl)cyclopentane. The 2-chloroethylamine was reacted with 2-methyl-4-nitrophenyl isocyanate according to Method C4a to afford 1-cyclohexyl-2-(2-methyl-4-nitrophenylimino)-3-oxa-1-azaspiro[4.4]nonane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353006B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-4bec818de8e34c649e9d1c55d689caf0
Quellennotizuspto-grants-2002_03