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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383839Generated: October 29, 2026

Sodium hydride → HCID 54398397, compound

https://huagongshe.com/reaction/1383839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant6-Chloro-3-phenyl[1,2,4]triazolo[4,3-b]pyridazineHCID 911462—
Reactant(1-methyl-1H-1,2,4-triazol-5-yl)methanolHCID 11073377—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 54398397HCID 54398397—

Reaction Steps

To a solution of (2-methyl-2 H-1,2,4-triazol-3-yl)methanol (0.9 g, 8.0 mmol) (prepared using the conditions described in EP-A-421210) in DMF (30 ml) was added sodium hydride (0.32 g of a 60% dispersion in oil, 1.6 mol eq.) and the reaction mixture was stirred at room temperature for 30 minutes. After this time the product from Example 88 Step a) (1.15 g, 5.0 mmol) was added as a solution in DMF (20 ml) and the reaction mixture was stirred at room temperature for 2 hours. The reaction mixture was diluted with water (200 ml) and the aqueous extracted with dichloromethane (4×150 ml). The combined extracts were dried (Na2SO4), filtered and evaporated. The residue was purified by chromatography on silica gel using 4% MeOH in dichloromethane as eluent to give the required product, (1.5 g, mp=254° C.). 1H NMR (360 MHz, CDCl3) δ3.98 (3 H, s), 5.61 (2 H, s), 6.90 (1 H, d, J=9.8 Hz), 7.51-7.60 (3 H, m), 7.94(1 H, s), 8.12 (1 H, d, J=9.8 Hz), 8.39 (2 H, dd, J=9.6, 1.5 Hz); MS (ES+) m/e 308 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255305B1
Source datasetuspto-grants-2001_07
ORD IDord-fe4fb98af2704abe9c566f21a437cb8f
Source noteuspto-grants-2001_07