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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276694Erstellt: 26. Oktober 2026

Ethanolamine → 13-aza-6-oxadispiro[4.2.4.I]tridecane

https://huagongshe.com/reaction/276694

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolamineHCID 700—
EduktCycloleucineHCID 2901—
EduktCyclopentanoneHCID 8452—
Edukt1-AminocyclopentanemethanolHCID 66307—
Produkt13-aza-6-oxadispiro[4.2.4.I]tridecaneHCID 18316287—

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 cyclopentanone according to Method B4d, Step 1 to give 6-aza-12-oxadispiro[4.1.4.2]tridecane. The oxazolidine was reduced according to Method B4d, Step 2 to give 1-(cyclopentylamino)-1-(hydroxymethyl)cyclopentane. The substituted 2-hydroxyethylamine was reacted with SOCl2 according to Method B7b to 1-(cyclopentylamino)-1-(chloromethyl)cyclopentane. The 2-chloroethylamine was reacted with 2-methyl-4-nitrophenyl isocyanate according to Method C4a to afford 1-cyclopentyl-2-(2-methyl-4-nitrophenylimino)-3-oxa-l-1-azaspiro[4.4]nonane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353006B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-01555bfe48344f7a8075ecf78d2b2163
Quellennotizuspto-grants-2002_03