HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → HCID 20363697, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | 3-Piperidin-3-yl-propylamine | HCID 12247576 | — |
| Reactant | HCID 12797296 | HCID 12797296 | — |
| Product | HCID 20363697 | HCID 20363697 | — |
Reaction Steps
For example, 3-(3-aminopropyl)piperidine may be converted to a Schiff base with 1,5-di-(4-isopropylphenyl)-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-(4-isopropylphenyl)-3-pentylamino]propyl}piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04079059 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-d86e62b99f4948a1aa82f067e59b2f2d |
| Source note | uspto-grants-1978_03 |