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HRID 474140作成日:2026年10月24日

Potassium Carbonate → (4-Pyrazolo[1,5-b]pyridazin-3-ylphenyl)acetic acid

https://huagongshe.com/reaction/474140

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetic AcidHCID 3719002—
反応物3-Bromopyrazolo(1,5-b)pyridazineHCID 52988024—
触媒palladium(II) acetateHCID 167845—
触媒2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物(4-Pyrazolo[1,5-b]pyridazin-3-ylphenyl)acetic acidHCID 5953594272%

反応手順

To a solution of 1.00 g (3.82 mmol) [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetic acid in 5.70 ml CH3CN and 3.80 ml water was added 0.76 g (3.82 mmol) 3-bromopyrazolo[1,5-b]pyridazine, 8.57 mg (0.038 mmol) palladium acetate, 1.21 g (8.77 mmol) potassium carbonate, and 0.031 g (0.076 mmol) SPhos. The resulting suspension was degassed for 5 minutes. After 30 min in the microwave at 150° C., the reaction mixture was cooled, acidified with 1N HCl, extracted with ethyl acetate, and washed with brine. The organic layer was dried over Na2SO4, filtered and concentrated in vacuo. Purification by flash chromatography (silica gel, linear gradient 50-100% EtOAc in hexanes) afforded 0.69 g (72%) (4-pyrazolo[1,5-b]pyridazin-3-ylphenyl)acetic acid. 1H NMR (CD3OD, 400 MHz) 8.40 (dd, J=1.83, 15.75 Hz, 1H); 8.40 (m, 1H); 8.28 (s, 1H); 7.62 (d, J=8.05 Hz, 2H); 7.41 (d, J=7.97 Hz, 2H); 7.22 (dd, J=4.4, 9.1 Hz, 1H); 3.66 (s, 2H). ES-MS M+1=254.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637513B2
出典データセットuspto-grants-2014_01
ORD IDord-2c2f6a5a0b39430b86692d9ef40f1ed5
出典メモuspto-grants-2014_01