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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625567Generated: October 30, 2026

Sodium ethoxide → 3-(2,4-Dimethylphenyl)-6-(pyridin-2-ylmethylthio)pyridazine

https://huagongshe.com/reaction/1625567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
Reactant2-(Bromomethyl)pyridine hydrobromideHCID 2734720—
Reactant6-(2,4-Dimethylphenyl)pyridazine-3-thiolHCID 12562100—
SolventEthanolHCID 702—
Product3-(2,4-Dimethylphenyl)-6-(pyridin-2-ylmethylthio)pyridazineHCID 4053204335%

Reaction Steps

To a mixture of 2-(bromomethyl)pyridine hydrobromide (116 mg; 0.46 mmol) and 6-(2,4-dimethylphenyl)pyridazine-3(2H)-thione (Example 13a) (100 mg, 0.46 mmol) in EtOH (3 mL) was added EtONa (20% in EtOH, 25 μl) and the reaction was irradiated in a microwave at 140° C. for 4 min. The crude mixture was dried down and purified on silica gel (Eluent: 5% MeOH in DCM) to give 3-(2,4-Dimethylphenyl)-6-(pyridin-2-ylmethylthio)pyridazine (49 mg, 35%) as a white solid solid. 1H NMR (300 MHz, dMSO: δ 2.49 (s, 3H), 2.54 (s, 3H), 4.09 (s, 2H), 6.32-6.37 (m, 2H), 6.45-6.52 (m, 2H), 6.75-6.78 (d, 1H), 6.84-6.87 (m, 2H), 6.95-6.98 (t, 1H), 7.67-7.68 (d, 1H); MS (M+H, 308).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08784782B2
Source datasetuspto-grants-2014_07
ORD IDord-bc417a0fa2314381892e6b2bbdaf4d76
Source noteuspto-grants-2014_07