HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276699Erstellt: 26. Oktober 2026
Ethanolamine → 13-aza-6-oxadispiro[4.2.4.I]tridecane
https://huagongshe.com/reaction/276699
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethanolamine | HCID 700 | — |
| Edukt | Cycloleucine | HCID 2901 | — |
| Edukt | Cyclopentanone | HCID 8452 | — |
| Edukt | 1-Aminocyclopentanemethanol | HCID 66307 | — |
| Produkt | 13-aza-6-oxadispiro[4.2.4.I]tridecane | HCID 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. 4-Amino-3-ethylbenzonitrile was converted to 4-cyano-2-ethylformanilide according to Method A3a, Step 1. The formanilide was reacted with SOCl2 and SO2Cl2 according to Method A3a, Step 2 to give 4-cyano-2-ethylphenyl isocyanide dichloride. The substituted 2-hydroxyethylamine was reacted with 2-methyl-4-nitrophenyl isocyanide dichloride according to Method C7a to afford 1-cyclopentyl-2-(2-methyl-4-nitrophenylimino)-3-oxa-1-azaspiro[4.4]nonane.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06353006B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-24f06a743e17471ba859c15d2e3ed75b |
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| Quellennotiz | uspto-grants-2002_03 |
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