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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333741Generated: October 30, 2026

Triphenylphosphine → 5-[3-(1-methyl-1H-benzimidazol-2-yl)propoxy]-3-(1-methyl-1H-pyrazol-5-yl)-1-phenylpyridazin-4(1H)-one

https://huagongshe.com/reaction/333741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant3-(1-Methyl-1H-benzimidazol-2-yl)propan-1-olHCID 4585215—
Reactant5-hydroxy-3-(1-methyl-1H-pyrazol-5-yl)-1-phenylpyridazin-4(1H)-oneHCID 89586758—
SolventTolueneHCID 1140—
Product5-[3-(1-methyl-1H-benzimidazol-2-yl)propoxy]-3-(1-methyl-1H-pyrazol-5-yl)-1-phenylpyridazin-4(1H)-oneHCID 8958647149.3%

Reaction Steps

Toluene (20 mL) was added to di-tert-butyl diazene-1,2-dicarboxylate (345 mg), and triphenylphosphine (459 mg) and the mixture was stirred at room temperature for 10 min. Then, 5-hydroxy-3-(1-methyl-1H-pyrazol-5-yl)-1-phenylpyridazin-4(1H)-one (268 mg), and further, 3-(1-methyl-1H-benzimidazol-2-yl)propan-1-ol (285 mg) were added, and the mixture was stirred at room temperature for 64 hr. The crystals precipitated from the reaction mixture were collected by filtration, washed successively with toluene, methanol, and diisopropyl ether, and dried to give the title compound (217 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883788B2
Source datasetuspto-grants-2014_11
ORD IDord-85e1babd8d854cf1b6ede54fcdd2f9d4
Source noteuspto-grants-2014_11