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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891942Generated: October 31, 2026

Dimethylformamide → HCID 22240125, compound

https://huagongshe.com/reaction/891942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-MethylimidazoleHCID 12749—
ReactantThionyl ChlorideHCID 24386—
Reactant[6-(3-Chloro-4-fluoro-phenyl)-pyridazin-4-yl]-methanolHCID 22240129—
SolventDichloromethaneHCID 6344—
ProductHCID 22240125HCID 2224012524.5%

Reaction Steps

[6-(3-Chloro-4-fluoro-phenyl)-pyridazin-4-yl]-methanol (13 mg, 0.054 mmol) was dissolved in MeCl2 (1 ml) under argon and a drop of DMF was added. The mixture was cooled with an icebath, thionylchloride (0.02 ml, 0.27 mmol) was added dropwise and the reaction mixture was allowed to warm to room temperature. After 30 minutes the reaction mixture was concentrated in vacuo. The residue was dissolved in ethanol and treated with 2-methyl-imidazole (22.3 mg, 0.27 mmol). The reaction mixture was refluxed for 12 hours then cooled to room temperature and concentrated. Ethyl acetate and a saturated NaHCO3 solution were added. The aqueous layer was extracted twice with ethyl acetate. The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo. The residue was chromatographed over silica gel (CH2Cl2—MeOH 19:1) to provide 3-(3-chloro-4-fluoro-phenyl)-5-(2-methyl-imidazol-1-yl-methyl)-pyridazine (4 mg, 24%) as a light brown oil, MS: m/e=303.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07005432B2
Source datasetuspto-grants-2006_02
ORD IDord-47ecde26c0744d60b5c5b78388bd47f7
Source noteuspto-grants-2006_02