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HRID 1624696作成日:2026年10月25日

Pyrazole → HCID 59436250、化合物

https://huagongshe.com/reaction/1624696

反応式

関与物質

役割名称HCID仕込み量
反応物PyrazoleHCID 1048—
反応物Salicylaldehyde oximeHCID 7200—
反応物Cesium carbonateHCID 10796—
反応物1-(4-iodo-2-methoxyphenyl)-N,5-dimethoxy-N-methyl-4-oxo-1,4-dihydropyridazine-3-carboxamideHCID 59436205—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物HCID 59436250HCID 5943625068.3%

反応手順

A suspension of 1-(4-iodo-2-methoxyphenyl)-N,5-dimethoxy-N-methyl-4-oxo-1,4-dihydropyridazine-3-carboxamide (10.7 g, 24 mmol), pyrazole (1.63 g, 24 mmol), Cu2O (0.343 g, 2.4 mmol), salicylaldoxime (1.32 g, 9.6 mmol), and Cs2CO3 (15.6 g, 48 mmol) in CH3CN (100 mL) was refluxed for 4 h under Ar atmosphere. After cooling to room temperature, the reaction mixture was poured into water and extracted with AcOEt. The extract was washed with brine, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography eluting with AcOEt/THF (1/0-0/1) to give the title compound (6.32 g, 68% yield) as a pale yellow amorphous solid: 1H NMR (300 MHz, CDCl3): δ ppm 3.39 (3H, s), 3.73 (3H, s), 3.91 (3H, s), 3.99 (3H, s), 6.53 (1H, dd, J=1.9, 2.3 Hz), 7.27 (1H, dd, J=2.3, 8.7 Hz), 7.58 (1H, d, J=8.7 Hz), 7.61 (1H, d, J=1.9 Hz), 7.77 (1H, d, J=1.5 Hz), 7.84 (1H, s), 7.98 (1H, d, J=2.3 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08778944B2
出典データセットuspto-grants-2014_07
ORD IDord-8500e9dd39614662a49104db3577bf64
出典メモuspto-grants-2014_07