Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Ethoxyaniline | HCID 9076 | — |
| Reactant | HCID 86611744 | HCID 86611744 | — |
| Reactant | HCID 86611745 | HCID 86611745 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86611743 | HCID 86611743 | — |
Reaction Steps
p-Phenetidine (0.068 g, 0.5 mmol) and triethylamine (0.15 ml, 1.1 mmol) were added to a mixture of 8-bromo-6-chloro-3-methylimidazo[1,2-b]pyridazine and 6,8-dichloro-3-methylimidazo[1,2-b]pyridazine (0.011 g, 0.5 mmol) both from 1a in EtOH (10 mL). The mixture was heated to 90° C. and stirred for 30 hrs. The solution was then concentrated in vacuo to give crude 6-chloro-N-(4-ethoxyphenyl)-3-methylimidazo[1,2-b]pyridazin-8-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07723336B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-cb48709c3f6c4075b97cc510ed4de2ab |
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| Source note | uspto-grants-2010_05 |
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