Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,5-Dichloro-3-hydroxypyridazine | HCID 73247 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 734445 | HCID 734445 | — |
Reaction Steps
A mixture of 7 g of 1-benzylpiperazine, 6.55 g of 4,5-dichloro-3(2H)-pyridazinone and 11 g of K2CO3 in 150 ml of DMF is heated at 110° C. for 4 hours and then concentrated under vacuum. The residue is chromatographed on silica gel, eluting with a DCM/MeOH (95/5; v/v) mixture. The product obtained is taken up in iso ether and triturated and the precipitate formed is isolated with suction. This gives 7 g of the expected product, which is recrystallized from iso ether; m.p.=173-175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468368B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-080e7e4b4f8d4107bde85394a9519f08 |
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| Source note | uspto-grants-2008_12 |
|---|