HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine-1-propylamine → HCID 15713319, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine-1-propylamine | HCID 19049 | — |
| Reactant | 1-Chloro-4-methylpyridazino[4,5-b]indolizine | HCID 15713312 | — |
| Product | HCID 15713319 | HCID 15713319 | — |
Reaction Steps
Following the procedure of Example 1, reaction of one equivalent of 1-chloro-4-methylpyridazino[4,5-b]indolizine and 10 equivalents of 1-(3-aminopropyl)piperidine at 130° C. gave the title compound as the free base (oil, 83%) after HPLC purification. Trituration with hexane gave a yellow solid (50%), mp 130°-134° C. The free base was then converted to the dihydrochloride salt (MeOH/ethereal HCl/diethyl ether), mp. 302°-303° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985560 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-a84022cdbf1c41aa84ff0e60701b1e39 |
| Source note | uspto-grants-1991_01 |