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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383829Generated: November 1, 2026

Sodium hydride → HCID 11462750, compound

https://huagongshe.com/reaction/1383829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant6-Methyl-2-pyridylmethanolHCID 70736—
Reactant6-chloro-3-phenyl-[1,2,4]triazolo[3,4-a]phthalazineHCID 1502563—
SolventDimethylformamideHCID 6228—
ProductHCID 11462750HCID 11462750—

Reaction Steps

To a solution of 2-hydroxymethyl-6-methylpyridine (Example 67 part b, 0.5 g), in anhydrous dimethylformamide (20 ml) under nitrogen was added sodium hydride (107 mg of 60% in oil) and the reaction mixture was stirred at room temperature for 0.5 hours. To this mixture was added 6-chloro-3-phenyl-1,2,4-triazolo[3,4-a]phthalazine (Example 67 part d, 330 mg) and the solution was heated to 80° C. for 0.25 hours. After cooling the solvent was removed under vacuum, and the residue was dissolved in dichloromethane (30 ml) and washed with water and brine. After drying (MgSO4), the solution was filtered and evaporated to give the required product which was recrystallised from a mixture of ethyl acetate and hexane to give the title compound (210 mg, m.p. 186-187° C.). 1H NMR (360 MHz, DMSO) δ 2.52 (3H, s), 5.65 (2H, s), 7.25 (1H, d, J=7.7Hz), 7.49 (1H, d, J=7.7Hz), 7.58 (3H, m), 7.76 (1H, t, J=7.7Hz), 7.94 (1H, t, J=7.6Hz), 8.08 (1H, t, J=7.7Hz), 8.30 (3H, m), 8.58 (1H, d, J=7.6Hz); MS (ES+) m/e 368 [MH]+. Anal. Found C, 71.32; H, 4.44; N. 18.53. C22H17N5O. H2O requires C, 71.22; H, 4.73; N, 18.88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255305B1
Source datasetuspto-grants-2001_07
ORD IDord-8d231c49cb6c4f8da8a1b7893839a279
Source noteuspto-grants-2001_07