HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276695Erstellt: 26. Oktober 2026
Ethanolamine → 5-Aza-12-oxadispiro[3.1.4.2]dodecane
https://huagongshe.com/reaction/276695
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanolamine | HCID 700 | — |
| Edukt | Cycloleucine | HCID 2901 | — |
| Edukt | Cyclobutanone | HCID 14496 | — |
| Edukt | 1-Aminocyclopentanemethanol | HCID 66307 | — |
| Produkt | 5-Aza-12-oxadispiro[3.1.4.2]dodecane | HCID 18315997 | — |
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 2-hydroxyethylamine was reacted with cyclobutanone according to Method B4a, Step 1 to give 5-aza-12-oxadispiro[3.1.4.2]dodecane. The oxazolidine was reduced according to Method B4a, Step 2 to give 1-(cyclobutylamino)-1-(hydroxymethyl)cyclopentane. The substituted 2-hydroxyethylamine was reacted with SOCl2 according to Method B7b to 1-(cyclobutylamino)-1-(chloromethyl)cyclopentane. The 2-chloroethylamine was reacted with 2-methyl-4-nitrophenyl isocyanate according to Method C4a to afford 1-cyclobutyl-2-(2-methyl-4-nitrophenylimino)-3-oxa-1-azaspiro[4.4]nonane.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06353006B1 |
|---|
| Quelldatensatz | uspto-grants-2002_03 |
|---|
| ORD ID | ord-b05a1cb0c8cf4b88846bcea17b61aa10 |
|---|
| Quellennotiz | uspto-grants-2002_03 |
|---|