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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447085Generated: October 30, 2026

Tetrahydrofuran → HCID 59191511, compound

https://huagongshe.com/reaction/447085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPyridine-2-acetonitrileHCID 75959—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant3,6-Dichloro-4,5-dimethylpyridazineHCID 21187505—
ProductHCID 59191511HCID 5919151144%

Reaction Steps

3,6-Dichloro-4,5-dimethyl-pyridazine (1.00 g, 5.65 mmol) is added to a dry 250-ml round-bottom flask under N2 followed by THF (50 mL) and pyridin-2-yl-acetonitrile (800 mg, 7.68 mmol). The reaction is degassed for 30 min. NaHMDS (1.0 M, 14.13 mL, 14.13 mmol) is added and the reaction is stirred overnight. The reaction mixture is transferred to a beaker and air stirred vigorously for several hours. The reaction mixture is quenched with saturated sodium bicarbonate solution. The organics are extracted with dichloromethane. The combined organic layers are washed with brine and dried over Na2SO4, filtered and concentrated under reduced pressure. The crude material is purified via flash chromatography on silica gel (0-20% methanol in CH2Cl2) to afford the title compound (616 mg, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481542B2
Source datasetuspto-grants-2013_07
ORD IDord-d83443d2c14e44e3be55b480b92cee33
Source noteuspto-grants-2013_07