HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097441Generated: October 30, 2026
2-(3-Cyclopropoxy-4-difluoromethoxyphenyl)-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one → HCID 135845022, compound
https://huagongshe.com/reaction/2097441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(3-Cyclopropoxy-4-difluoromethoxyphenyl)-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one | HCID 66602461 | — |
| Reactant | HCID 66602845 | HCID 66602845 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 135845022 | HCID 135845022 | 65% |
Reaction Steps
Reaction was carried out in the same manner as in Example 1-(b) except for using 581 mg (1.06 mmol) of 2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-3-cyclopropylmethoxymethyl-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo-[2,3-d]pyridazin-4-one obtained in Example 59-(a) in place of 2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one. After completion of the reaction, the reaction mixture was concentrated under reduced pressure, water was added to the obtained concentrate, and precipitated solid was collected by filtration and washed with water. The obtained crude solid was applied to silica gel column chromatography (Eluent; ethyl acetate), and the fractions containing the desired compound were concentrated under reduced pressure to obtain 287 mg of the title compound as a white solid. (Yield: 65%)
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-9bea9cf2e2cc480283b59900c2b87dba |
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| Source note | uspto-grants-2013_05 |
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