HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805587Generated: October 31, 2026
HCID 58072406, compound → HCID 58072486, compound
https://huagongshe.com/reaction/1805587
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 58072406 | HCID 58072406 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58072486 | HCID 58072486 | 92% |
Reaction Steps
A solution of 1-(2,3-difluoro-4-morpholin-4-ylphenyl)-N,5-dimethoxy-N-methyl-4-oxo-1,4-dihydropyridazine-3-carboxamide (1.1 g, 2.6 mmol) in THF (25 mL) was added dropwise to MeMgBr (1.0 M in THF, 11 mL, 11 mmol) at −78° C. under N2. The mixture was stirred at −78° C. for 1 h. The reaction was quenched with 1 M HCl aqueous solution (11 mL) at −78° C. The mixture warmed up to room temperature, diluted with AcOEt, and washed with brine. The organic layer was dried over MgSO4, and concentrated under reduced pressure. The residue was recrystallized from iPr2O/AcOEt to give the title compound (870 mg, 92% yield) as a pale yellow solid: 1H NMR (300 MHz, DMSO-d6): δ ppm 2.49 (3H, s), 2.90-3.28 (4H, m), 3.64-4.01 (7H, m), 7.05 (1H, td, J=8.9, 2.3 Hz), 7.53 (1H, td, J=8.6, 2.5 Hz), 8.50 (1H, d, J=1.9 Hz). LC-MS (ESI) m/z 366 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354411B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-ee47b2a5a6334bc1bce397b1df2db524 |
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| Source note | uspto-grants-2013_01 |
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