HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloro-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one → 2-(8-Difluoromethoxy-2,2-dimethyl-2H-chromen-5-yl)-3-ethyl-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one HCl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloro-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one | HCID 66602634 | — |
| Reactant | 2-(8-difluoromethoxy-2,2-dimethyl-2H-chromen-5-yl)-3-ethyl-5-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one | HCID 136337352 | — |
| Product | 2-(8-Difluoromethoxy-2,2-dimethyl-2H-chromen-5-yl)-3-ethyl-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one HCl | HCID 136346675 | 93% |
Reaction Steps
Reaction was carried out in the same manner as in Example 6-(c) except for using 613 mg (1.18 mmol) of 2-(8-difluoromethoxy-2,2-dimethyl-2H-chromen-5-yl)-3-ethyl-5-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one obtained in Example 54-(b) in place of 3-chloro-2-(3-cyclopropoxy-4-difluoromethoxyphenyl)-1-(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one. After completion of the reaction, the solid obtained from the reaction suspension by filtration was washed with hexane and dried under reduced pressure to obtain 467 mg of the title compound as a white solid. (Yield: 93%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450319B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-c4f3528ae270487ba5ee0c0aa7a4456e |
| Source note | uspto-grants-2013_05 |