HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515556Generated: October 29, 2026
Pyridazine → Ethyl 4-[6-chloro-2-(4-fluorophenyl)-imidazo[1,2-b]pyridazin-3-yl]-4H-pyridazine-1-carboxylate
https://huagongshe.com/reaction/515556
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridazine | HCID 9259 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 6-Chloro-2-(4-fluorophenyl)imidazo[1,2-b]pyridazine | HCID 11436572 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-[6-chloro-2-(4-fluorophenyl)-imidazo[1,2-b]pyridazin-3-yl]-4H-pyridazine-1-carboxylate | HCID 59367707 | — |
Reaction Steps
2.90 ml (30.3 mmol) of ethyl chloroformate are added, dropwise in 30 minutes, to a solution of 3.00 g (12.1 mmol) of 6-chloro-2-(4-fluorophenyl)imidazo[1,2-b]pyridazine (CAS: 244081-70-7) and 4.40 ml (60.6 mmol) of pyridazine in 40 ml of dichloromethane at 10° C. The medium is stirred at 10° C. for a further hour and then left to stir for 3 hours. It is then poured into ice-cold water and the product is extracted with ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108971B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-8e7fa7b1880a4635a86e1f0e085bc3c5 |
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| Source note | uspto-grants-2015_08 |
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