HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244263Generated: October 30, 2026
Potassium Carbonate → 6-Chloro-3-[2-(6-fluoro-pyridin-2-yl)-imidazol-1-ylmethyl]-4-propyl-pyridazine
https://huagongshe.com/reaction/1244263
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoro-6-(1h-imidazol-2-yl)pyridine | HCID 21919286 | — |
| Reactant | 6-Chloro-3-chloroethyl-4-propyl-pyridazine | HCID 85991334 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Chloro-3-[2-(6-fluoro-pyridin-2-yl)-imidazol-1-ylmethyl]-4-propyl-pyridazine | HCID 10382055 | — |
Reaction Steps
DMF (30 ml) is added to a mixture of 6-chloro-3-chloroethyl-4-propyl-pyridazine (5.01 g, 24.43 mmol), 2-fluoro-6-(imidazol-2-yl)-pyridine (3.99 g, 24.43 mmol) and anhydrous K2CO3 (10.2 g, 73.3 mmol) and the mixture is stirred at room temperature overnight. The solvent is removed in vacuo, water (30 ml) and EtOAc (30 ml) are added to the residue and the layers are separated. The aqueous layer is extracted with EtOAc (3×30 ml) and the combined extracts are washed with brine (30 ml), dried (Na2SO4) and evaporated, which provides a light brown solid. The solid is washed twice with 1:1 hexane, ether (25 ml), which provides the title compound as a light yellow solid. 1H NMR (CDCl3) 8.12–8.15 (m, 1H), 7.84 (q, 1H), 7.32 (s, 1H), 7.17 (d, 1H), 7.10 (d, 1H), 6.81–6.84 (m, 1H), 6.22 (s, 2H), 2.68 (t, 2H), 1.54–1.62 (m, 2H), 0.91 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07122546B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-be3c7eed18f14b65a511ce9a9174c580 |
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| Source note | uspto-grants-2006_10 |
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