HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239840Generated: October 31, 2026
Chloroacetaldehyde → 8-Bromo-6-chloro-7-phenylimidazo[1,2-b]pyridazine hydrochloride
https://huagongshe.com/reaction/2239840
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | 4-Bromo-6-chloro-5-phenylpyridazin-3-amine | HCID 86611723 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 8-Bromo-6-chloro-7-phenylimidazo[1,2-b]pyridazine hydrochloride | HCID 86611721 | 94% |
Reaction Steps
Chloroacetaldehyde (2.0 mL, 31.5 mmol) was added to a solution of crude 4-bromo-6-chloro-5-phenylpyridazin-3-amine (0.193 g, 0.676 mmol) from 1b in EtOH (5.0 mL). The mixture was heated in a sealed tube at 118° C. for 5 h. After cooling to room temperature, the reaction mixture was concentrated in vacuo, and suspended in acetone/Et2O (1:1, 3 mL), filtered, and washed with Et2O to give 8-bromo-6-chloro-7-phenylimidazo[1,2-b]pyridazine HCl salt (0.147 g, >94% purity).
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-8794c8292d6f44f4b95ebc0f4ac8f72e |
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| Source note | uspto-grants-2010_05 |
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