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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 403370생성일: 2026년 10월 24일

Sodium Carbonate → 6-Chloro-4-(4-fluoro-2-methoxy-phenyl)-pyridazin-3-ylamine

https://huagongshe.com/ko/reaction/403370

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물TriphenylphosphineHCID 11776—
반응물Sodium BicarbonateHCID 516892—
반응물(4-Fluoro-2-methoxyphenyl)boronic acidHCID 2782672—
반응물3-Amino-4-bromo-6-chloropyridazineHCID 22024419—
용매1,2-DimethoxyethaneHCID 8071—
용매Ethyl AcetateHCID 8857—
생성물6-Chloro-4-(4-fluoro-2-methoxy-phenyl)-pyridazin-3-ylamineHCID 86698475—

반응 단계

To a solution of 4-bromo-6-chloropyridazin-3-amine (2.5 g, 12.0 mmol, CAS RN 446273-59-2) in 1,2-dimethoxyethane (30 mL) was added 4-fluoro-2-methoxyphenylboronic acid (2.45 g, 14.4 mmol, CAS RN 179899-07-1) and 2M aqueous sodium carbonate solution (10 mL). The reaction mixture was stirred under argon atmosphere for 15 minutes. Pd(II)acetate (135 mg, 600 μmol) and triphenylphosphine (315 mg, 1.2 mmol) was added. The dark red reaction mixture was stirred at 90° C. for 8 hours and then poured on 10% aqueous sodium bicarbonate solution (200 mL) and ethyl acetate (200 mL), filtered over dicalite and the layers were separated. The aqueous layer was extracted a second time with ethyl acetate (200 mL). The organic layers were washed with 200 mL brine, dried over magnesium sulfate, filtered and concentrated under vacuum. The residue was purified by silica gel chromatography on a 120 g column using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of n-heptane:ethyl acetate (100:0 to 0:100). Light red solid (1.71 g, 56.2%). MS (ESI+): m/z=254.050 ([M+H]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748434B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-0e1a5ff536574a21ae0f04680c37513e
출처 메모uspto-grants-2014_06