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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402403Generated: October 30, 2026

Sodium hydride → 3-Chloro-6-(3-methyl-5-pyridin-2-yl-3H-[1,2,3]triazol-4-ylmethoxy)-pyridazine

https://huagongshe.com/reaction/402403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3,6-DichloropyridazineHCID 67331—
Reactant(3-methyl-5-pyridin-2-yl-3H-[1,2,3]triazol-4-yl)-methanolHCID 67498007—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-6-(3-methyl-5-pyridin-2-yl-3H-[1,2,3]triazol-4-ylmethoxy)-pyridazineHCID 5733509799.1%

Reaction Steps

To a suspension of sodium hydride (55%, 92 mg, 2.10 mmol) in THF (3 mL) was added a solution of (3-methyl-5-pyridin-2-yl-3H-[1,2,3]triazol-4-yl)-methanol (400 mg, 2.103 mmol) in THF (5 mL) under ice cooling. The mixture was then allowed to warm up to room temperature and stirred for 30 min. Again under ice cooling was added a solution of 3,6-dichloropyridazine (315 mg, 2.10 mmol) in THF (5 mL) and the resulting mixture stirred at room temperature for 16 h. The mixture was then poured into ice water and extracted with ethyl acetate and the combined organic extracts washed with brine, dried over sodium sulphate, filtered and evaporated. Purification by chromatography (silica, 0 to 50% ethyl acetate in heptane) afforded the title compound (630 mg, 99%) as a white solid. MS: m/e=303.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742097B2
Source datasetuspto-grants-2014_06
ORD IDord-8aeeaff01a9549d0ae35fa71bc34faa7
Source noteuspto-grants-2014_06