HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bicyclo[3.2.1]octan-2-one → N-(Bicyclo[3.2.1]oct-2-yl)-N'-(4-methylpyridazino[4,5-b]indolizin-1-yl) 1,2-ethanediamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bicyclo[3.2.1]octan-2-one | HCID 107363 | — |
| Reactant | HCID 20075511 | HCID 20075511 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethyl sulfoxide methanol | HCID 22036561 | — |
| Product | N-(Bicyclo[3.2.1]oct-2-yl)-N'-(4-methylpyridazino[4,5-b]indolizin-1-yl) 1,2-ethanediamine | HCID 20075513 | — |
Reaction Steps
Following the procedure of Example 12, bicyclo[3.2.1]octan-2-one in methanol (3 to 4 mL) was added to a solution of N-(4-methylpyridazino[4,5-b]indolizin-1-yl)-1,2-ethanediamine hydrochloride in methanol/DMSO (90 mL:30 mL) which had been heated to boiling and then allowed to cool. After stirring at room temperature overnight, the title compound was obtained as the free base after column chromatography (silica gel, 4:1 methylene chloride:methanol to 100% methanol containing ammonium hydroxide) and recrystallized from isopropyl ether. The compound was converted to the dihydrochloride salt by ethanolic HCl, mp 339°-344° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985560 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-af0ce9f90e2948de88d97fd7b1f2795a |
| Source note | uspto-grants-1991_01 |