HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromopentane → 2-(4-Cyano-2-ethylphenylimino)-1-(3-pentyl)-3-thia-1-azaspiro[4.4]nonane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromopentane | HCID 15738 | — |
| Reactant | HCID 178436586 | HCID 178436586 | — |
| Product | 2-(4-Cyano-2-ethylphenylimino)-1-(3-pentyl)-3-thia-1-azaspiro[4.4]nonane | HCID 18316368 | — |
Reaction Steps
1-Hydroxymethylcyclopentanamine was prepared according to Method B1c. The 2-hydroxyethylamine was converted to 1-chloromethylcyclopentanamine HCl salt according to Method B7e. 1-Chloromethylcyclopentanamine HCl salt was reacted with 4-cyano-2-ethylphenyl isothiocyanate according to Method C1e to give 2-(4-cyano-2-ethylphenylimino)-3-thia-1-azaspiro[4.4]nonane. The thiazolidine was reacted with 3-bromopentane according to Method D2b to give 2-(4-cyano-2-ethylphenylimino)-1-(3-pentyl)-3-thia-1-azaspiro[4.4]nonane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353006B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-99b15b0472434bb480ff2bf0ee467872 |
| Source note | uspto-grants-2002_03 |