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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Benzyloxymethyl-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-3-(6-methoxy-3-pyridylmethyl)-1,5-dihydropyrrolo[2,3-d]-pyridazin-4-one | HCID 66602760 | — |
| Reactant | HCID 66602968 | HCID 66602968 | — |
| Product | 2-(3-Cyclopropoxy-4-difluoromethoxyphenyl)-3-(6-methoxy-3-pyridylmethyl)-1,5-dihydropyrrolo[2,3-d]-pyridazin-4-one | HCID 135845048 | 69% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08450319B2 |
|---|
| Source dataset | uspto-grants-2013_05 |
|---|
| ORD ID | ord-3b299a7703814a9e87e09358528499ea |
|---|
| Source note | uspto-grants-2013_05 |
|---|