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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12297Generated: October 26, 2026

Ethanol → 4-(1H-Benzimidazol-2-yl)-6-(2-cyclopropylpyrimidin-4-yl)-2H-pyridazin-3-one

https://huagongshe.com/reaction/12297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant6-(2-Cyclopropylpyrimidin-4-yl)-2-(2-trimethylsilanylethoxymethyl)-4-[1-(2-trimethylsilanylethoxymethyl)-1H-benzimidazol-2-yl]-2H-pyridazin-3-oneHCID 68679877—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
Product4-(1H-Benzimidazol-2-yl)-6-(2-cyclopropylpyrimidin-4-yl)-2H-pyridazin-3-oneHCID 135978791—

Reaction Steps

27 mg of 6-(2-cyclopropylpyrimidin-4-yl)-2-(2-trimethylsilanylethoxymethyl)-4-[1-(2-trimethylsilanylethoxymethyl)-1H-benzimidazol-2-yl]-2H-pyridazin-3-one are dissolved in 2.5 ml of 4M hydrochloric acid solution in dioxane and 1 ml of ethanol and stirred at room temperature for 2 days. The solvent is then distilled off, and the residue is dissolved in 2 ml of dichloromethane and 1 ml of trifluoroacetic acid and again stirred at room temperature for 3 h. Distillation off is then repeated, and the residue is dissolved in 1 ml of 2M sodium hydroxide solution and 2 ml of water, and the mixture is stirred at room temperature for 10 h. For workup, it is neutralized with 2M hydrochloric acid, the volatile components are distilled off, and the crude product is purified by RP HPLC (acetonitrile (+0.05% HCOOH)/water (+0.05% HCOOH)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727989B2
Source datasetuspto-grants-2010_06
ORD IDord-836e08e052fe43058a58ca664df681f1
Source noteuspto-grants-2010_06