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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 474140생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/474140

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetic AcidHCID 3719002—
반응물3-Bromopyrazolo(1,5-b)pyridazineHCID 52988024—
촉매palladium(II) acetateHCID 167845—
촉매2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물(4-Pyrazolo[1,5-b]pyridazin-3-ylphenyl)acetic acidHCID 5953594272%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637513B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-2c2f6a5a0b39430b86692d9ef40f1ed5
출처 메모uspto-grants-2014_01