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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447084Generated: October 30, 2026

Tetrahydrofuran → HCID 59191601, compound

https://huagongshe.com/reaction/447084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3-PyridineacetonitrileHCID 80923—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant3,6-Dichloro-4,5-dimethylpyridazineHCID 21187505—
ProductHCID 59191601HCID 5919160193%

Reaction Steps

3,6-Dichloro-4,5-dimethyl-pyridazine (1.00 g, 5.65 mmol) is added to an oven-dried, 250-mL round-bottom flask under N2 followed by THF (50 mL) and pyridin-3-yl-acetonitrile (800 mg, 7.68 mmol). The reaction is degassed with a flow of N2 for 30 min. NaHMDS (14.13 mL, 1.0 M, 14.13 mmol) is added and the reaction is stirred for 16 h. The reaction mixture is then transferred to a beaker and stirred vigorously under open to the atmosphere for several hours. The reaction is quenched with saturated sodium bicarbonate solution, and the organics are extracted with dichloromethane. The combined organic layers are washed with brine, 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 (1.3 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481542B2
Source datasetuspto-grants-2013_07
ORD IDord-279f87c76d4741e59c9bfd19628f68b0
Source noteuspto-grants-2013_07