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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097400Generated: October 31, 2026

2-(3-Cyclopropoxy-4-difluoromethoxyphenyl)-3-propyl-5-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one → 2-(3-Cyclopropoxy-4-difluoromethoxyphenyl)-3-phenethyl-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one

https://huagongshe.com/reaction/2097400

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Cyclopropoxy-4-difluoromethoxyphenyl)-3-propyl-5-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-oneHCID 136346667—
Reactant2-(3-Cyclopropoxy-4-difluoromethoxyphenyl)-3-phenethyl-5-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-oneHCID 136346669—
Product2-(3-Cyclopropoxy-4-difluoromethoxyphenyl)-3-phenethyl-1,5-dihydropyrrolo[2,3-d]pyridazin-4-oneHCID 13584504980%

Reaction Steps

Reaction was carried out in the same manner as in Example 6-(c) except for using 364 mg (0.641 mmol) of 2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-3-phenethyl-5-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one obtained in Example 21-(b) in place of 2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-5-(2-trimethylsilylethoxymethyl)-3-propyl-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one. After completion of the reaction, the solid was collected by filtration from the reaction suspension and washed with 1,4-dioxane. To the obtained solid were added methanol and 28% aqueous ammonia, and the mixture was stirred at room temperature for 16 hours. Then, water was added to the solution, and the precipitated solid was collected by filtration. The obtained solid was washed with water and dried under reduced pressure to obtain 224 mg of the title compound as a white solid. (Yield: 80%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450319B2
Source datasetuspto-grants-2013_05
ORD IDord-ada525026f704989a123067bb645eac0
Source noteuspto-grants-2013_05