HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097406Generated: November 1, 2026
1-Benzyloxymethyl-3-(3-carboxybenzyl)-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one → 3-(3-Carboxybenzyl)-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one
https://huagongshe.com/reaction/2097406
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Benzyloxymethyl-3-(3-carboxybenzyl)-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one | HCID 66602783 | — |
| Reactant | HCID 66602968 | HCID 66602968 | — |
| Product | 3-(3-Carboxybenzyl)-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one | HCID 135845043 | 82% |
Reaction Steps
Reaction was carried out in the same manner as in Example 22-(b) except for using 1.05 g (1.79 mmol) of 1-benzyloxymethyl-3-(3-carboxybenzyl)-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one obtained in Example 27-(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 mixture was extracted with an alkaline aqueous solution with a pH 10, washed with diethyl ether, and after adjusting a pH of the aqueous layer to 2, the precipitated solid was collected by filtration. The obtained solid was washed with water and dried under reduced pressure to obtain 0.68 g of the title compound as a beige solid. (Yield: 82%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450319B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-bdead645505047be89d9935a47d7e2f0 |
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| Source note | uspto-grants-2013_05 |
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