HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895151Generated: October 29, 2026
HCID 86643933, compound → HCID 59436162, compound
https://huagongshe.com/reaction/1895151
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86643933 | HCID 86643933 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59436162 | HCID 59436162 | 99% |
Reaction Steps
To a solution of 1-(2,2-difluoro-1,3-benzodioxol-4-yl)-N,5-dimethoxy-N-methyl-4-oxo-1,4-dihydropyridazine-3-carboxamide (2.7 g, 7.2 mmol) in THF (70 mL) was added dropwise 1 M MeMgBr in THF (14 mL, 14 mmol) at −78° C. for 15 min. After stirring at −78° C. for 1 h, the mixture was quenched with 1 M HCl aqueous solution (30 mL). The mixture was warmed to room temperature and extracted with AcOEt. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound (2.3 g, 99% yield) as yellow crystals: 1H NMR (300 MHz, CDCl3): δ ppm 2.69 (3H, s), 3.95 (3H, s), 7.17 (1H, dd, J=7.9, 1.1 Hz), 7.26-7.32 (1H, m), 7.55 (1H, dd, J=8.7, 1.1 Hz), 8.00 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513251B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-26eab59139784dd0a25460c0b03f2742 |
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| Source note | uspto-grants-2013_08 |
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