HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → HCID 21425715, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | 3-Piperidin-3-yl-propylamine | HCID 12247576 | — |
| Reactant | HCID 21425721 | HCID 21425721 | — |
| Product | HCID 21425715 | HCID 21425715 | — |
Reaction Steps
For example, 3-(3-aminopropyl)piperidine may be converted to a Schiff base with 1,5-di-(3-isopropylnorborn-2-yl)-3-pentanone, catalytically reduced, then the resulting amine selectively cyanoethylated on the ring nitrogen with acrylonitrile, followed by catalytic hydrogenation to furnish 1-(3-aminopropyl)-3-{3-[1,5-di-(3-isopropylnorborn-2-yl)-3-pentylamino]propyl}piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04033748 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-8605dac52ee444388423bc96e9f1aabd |
| Source note | uspto-grants-1977_07 |