HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 4-Methyl-N-[2-(1-methyl-2-pyrrolidinyl)ethyl]pyridazino[4,5-b]indolizin-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-(2-Aminoethyl)-1-methylpyrrolidine | HCID 98388 | — |
| Reactant | 1-Chloro-4-methylpyridazino[4,5-b]indolizine | HCID 15713312 | — |
| Product | 4-Methyl-N-[2-(1-methyl-2-pyrrolidinyl)ethyl]pyridazino[4,5-b]indolizin-1-amine | HCID 15713329 | — |
Reaction Steps
Following the procedure of Example 1, reaction of one equivalent of 1-chloro-4-methylpyridazino[4,5-b]indolizine, ten equivalents of 2-(1-methyl-2-pyrrolidinyl)ethylamine and one equivalent of ammonium chloride under reflux in a nitrogen atmosphere for 3 to 4 hours gave the title compound as the free base after removal of excess amine in vacuo and treatment of the residue with boiling ethyl acetate. The solid collected upon filtration was converted to the hydrochloride salt (methanol/ethereal HCl/ether), mp 169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985560 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-58b54f67740a41858f44b5cf6b921848 |
| Source note | uspto-grants-1991_01 |