HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-chloro-N-(4-nitrophenyl)imidazo[1,2-b]pyridazin-8-amine → HCID 178511634, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-chloro-N-(4-nitrophenyl)imidazo[1,2-b]pyridazin-8-amine | HCID 86611730 | — |
| Reactant | HCID 178511674 | HCID 178511674 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178511634 | HCID 178511634 | — |
Reaction Steps
In a 2 dram reaction vial was added crude 6-chloro-N-(4-nitrophenyl)imidazo[1,2-b]pyridazin-8-amine (0.42 g, 1.4 mmol) from 1a and trans-1,4-diaminocyclohexane (1.0 g, 8.0 mmol). The mixture was allowed to melt at 160° C. for 8 hrs. The melt was then cooled, diluted with water and extracted with dichloromethane. The organic layer was concentrated to provide crude N6-((trans)-4-aminocyclohexyl)-N8-(4-nitrophenyl)imidazo[1,2-b]pyridazine-6,8-diamine which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723336B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-995372ea6b4a41dd958deb000c2d19ea |
| Source note | uspto-grants-2010_05 |