HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088366Generated: October 30, 2026
Chlorotrimethylsilane → HCID 59534566, compound
https://huagongshe.com/reaction/2088366
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | HCID 59534591 | HCID 59534591 | — |
| Catalyst | Tetrabutylammonium nitrite | HCID 3015282 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59534566 | HCID 59534566 | — |
Reaction Steps
37.2 1.14 ml (9.00 mmol) of trimethylchlorosilane are added to a suspension of 381 mg (1.00 mmol) of 2-[3-(5-amino-1,2,4-oxadiazol-3-yl)-benzyl]-6-(3,5-difluorophenyl)-2H-pyridazin-3-one in 5 ml of dichloromethane. A solution of 865 mg (3.00 mmol) of tetrabutylammonium nitrite in 3 ml of dichloromethane is slowly added dropwise to this suspension at room temperature with stirring. After the reaction mixture has been stirred at room temperature for 16 hours, it is filtered. The filtrate is partitioned between dilute sodium hydrogencarbonate solution and dichloromethane. The organic phase is dried over sodium sulfate and evaporated, giving crude 2-[3-(5-chloro-1,2,4-oxadiazol-3-yl)benzyl]-6-(3,5-difluorophenyl)-2H-pyridazin-3-one as yellowish oil, which is employed for the next reaction without further purification; ESI 401.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08435981B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-f40f29cf912c4bc9b28dbebe5d6ec10c |
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| Source note | uspto-grants-2013_05 |
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