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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Chloroethylamine | HCID 13369 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 2-Methyl-4-nitrophenyl isocyanate | HCID 4296456 | — |
| Edukt | 1-(Cyclohexylamino)-1-(chloromethyl)cyclopentane | HCID 18316166 | — |
| Produkt | 1-Cyclohexyl-2-(2-methyl-4-nitrophenylimino)-3-oxa-1-azaspiro[4.4]nonane | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06353006B1 |
|---|
| Quelldatensatz | uspto-grants-2002_03 |
|---|
| ORD ID | ord-4bec818de8e34c649e9d1c55d689caf0 |
|---|
| Quellennotiz | uspto-grants-2002_03 |
|---|