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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306591Generated: October 30, 2026

Sodium hydride → HCID 22609942, compound

https://huagongshe.com/reaction/2306591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(1-methyl-1H-1,2,4-triazol-5-yl)methanolHCID 11073377—
ReactantHCID 22609939HCID 22609939—
SolventDimethylformamideHCID 6228—
ProductHCID 22609942HCID 2260994230%

Reaction Steps

Sodium hydride (60% dispersion in oil, 16 mg, 0.41 mmol) was added to a solution of (2-methyl-2H-1,2,4-triazol-3-yl)methanol (prepared using the conditions described in EP-A-421210) (38 mg, 0.33 mmol) in dry DMF (2 ml) at room temperature. After 1 h at room temperature a solution of 6-chloro-3-(2,4-difluorophenyl)-7-(pyrrolidin-1-yl)-1,2,4-triazolo[4,3-b]pyridazine (102 mg, 0.30 mmol) was added and the reaction stirred for 18 hours. The residue was partitioned between dichloromethane and water. The aqueous was further extracted with dichloromethane (2×100 ml). The combined extracts were dried (Na2SO4), filtered and evaporated. The residue was purified by chromatography on silica gel, eluting with 0-2% ethyl acetate-methanol to afford the title pyridazine (42 mg, 30%). 1H NMR (250 MHz, CDCl3) 1.73-1.78 (4H, m), 3.51-3.55 (4H, m), 3.93 (3H, s), 5.40 (2H, s), 6.65 (1H, s), 6.95-7.03 (2H, m), 7.92-7.94 (1H, m), 8.04 (1H, s), MS (ES+) 413 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828322B2
Source datasetuspto-grants-2004_12
ORD IDord-dc852d26116d4f308acbf8e7226f73ec
Source noteuspto-grants-2004_12