HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522501Generated: October 30, 2026
3,6-Dichloropyridazine → HCID 14143072, compound
https://huagongshe.com/reaction/522501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14143072 | HCID 14143072 | 96% |
Reaction Steps
3,6-Dichloropyridazine (3) (149 mg, 1.0 mmol) in THF (2 mL) was added to a solution of TMPZnCl.LiCl (2) (1.3 M in THF, 0.85 mL, 1.1 mmol) at 25° C. and the reaction mixture was then stirred at this temperature for 30 min according to TP 2. After cooling down to −20° C., CuCN.2LiCl (1.0 M in THF, 1.1 mmol, 1.1 equiv) was added and the resulting mixture was stirred for 30 min at this temperature. 4-Fluorobenzoyl chloride (317 mg, 2.0 mmol) was then slowly added and the resulting mixture was allowed to warm up slowly to 10° C. The reaction mixture was quenched with a sat. aq. NH4Cl solution (20 mL), extracted with diethyl ether (3×50 mL) and dried over anhydrous Na2SO4. After filtration, the solvent was evaporated in vacuo. Purification by flash-chromatography (CH2Cl2/n-pentane, 1:1) furnished compound 5b (259 mg, 96%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334237B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-d4012b8b41a6411ca52358db9b1cce57 |
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| Source note | uspto-grants-2016_05 |
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