HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(3-Azabicyclo[3.2.2]non-3-yl)butylamine → N-[4-(3-Azabicyclo[3.2.2]non-3-yl)butyl]-6,7,8,9-tetrahydro-4-methylpyridazino[4,5-b]indolizin-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(3-Azabicyclo[3.2.2]non-3-yl)butylamine | HCID 13511081 | — |
| Reactant | 1-Chloro-4-methyl-6,7,8,9-tetrahydropyridazino[4,5-b]indolizine | HCID 86752616 | — |
| Product | N-[4-(3-Azabicyclo[3.2.2]non-3-yl)butyl]-6,7,8,9-tetrahydro-4-methylpyridazino[4,5-b]indolizin-1-amine | HCID 9842921 | — |
Reaction Steps
Following the procedure in Example 9, compound XII was allowed to react with 4-(3-azabicyclo[3.2.2]non-3-yl)butylamine to give the title compound which was converted to the dihydrochloride salt: m.p.210° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05756501 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-bee5ec45d8a545a4b5f557a978972860 |
| Source note | uspto-grants-1998_05 |