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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097408Generated: October 31, 2026

1-Benzyloxymethyl-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-3-(6-methoxy-3-pyridylmethyl)-1,5-dihydropyrrolo[2,3-d]-pyridazin-4-one → 2-(3-Cyclopropoxy-4-difluoromethoxyphenyl)-3-(6-methoxy-3-pyridylmethyl)-1,5-dihydropyrrolo[2,3-d]-pyridazin-4-one

https://huagongshe.com/reaction/2097408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyloxymethyl-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-3-(6-methoxy-3-pyridylmethyl)-1,5-dihydropyrrolo[2,3-d]-pyridazin-4-oneHCID 66602760—
ReactantHCID 66602968HCID 66602968—
Product2-(3-Cyclopropoxy-4-difluoromethoxyphenyl)-3-(6-methoxy-3-pyridylmethyl)-1,5-dihydropyrrolo[2,3-d]-pyridazin-4-oneHCID 13584504869%

Reaction Steps

Reaction was carried out in the same manner as in Example 22-(b) except for using 265 mg (1.79 mmol) of 1-benzyloxymethyl-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-3-(6-methoxy-3-pyridylmethyl)-1,5-dihydropyrrolo[2,3-d]-pyridazin-4-one obtained in Example 29-(a) in place of 1-benzyloxymethyl-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-3-(2-fluorobenzyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one. After completion of the reaction, the reaction suspension was filtered, the filtrate was concentrated under reduced pressure, methanol and 28% aqueous ammonia were added to the obtained solid, and the mixture was stirred for 1 hour. Then, the solution was concentrated under reduced pressure and the obtained residue was applied to silica gel column chromatography (Eluent; ethyl acetate), and the fractions containing the desired compound were concentrated under reduced pressure to obtain 146 mg of the title compound as a white solid. (Yield: 69%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450319B2
Source datasetuspto-grants-2013_05
ORD IDord-3b299a7703814a9e87e09358528499ea
Source noteuspto-grants-2013_05