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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1348778생성일: 2026년 10월 26일

Pyridine → 4-bromomethyl-2-cyclopropylmethyl-6-(3-fluoro-4-methoxyphenyl)-2H-pyridazin-3-one

https://huagongshe.com/reaction/1348778

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Carbon tetrabromideHCID 11205—
반응물TriphenylphosphineHCID 11776—
반응물2-cyclopropylmethyl-6-(3-fluoro-4-methoxyphenyl)-4-hydroxymethyl-2H-pyridazin-3-oneHCID 21991643—
용매TetrahydrofuranHCID 8028—
생성물4-bromomethyl-2-cyclopropylmethyl-6-(3-fluoro-4-methoxyphenyl)-2H-pyridazin-3-oneHCID 2199171069.5%

반응 단계

2-Cyclopropylmethyl-6-(3-fluoro-4-methoxyphenyl)-4-hydroxymethyl-2H-pyridazin-3-one (185 mg, 0.61 mmol), carbon tetrabromide (404 mg, 1.2 mmol) and pyridine (48 mg, 0.61 mmol) were dissolved in tetrahydrofuran (3 mL), and under ice-cold stirring, a solution of triphenylphosphine (319 mg, 1.2 mmol) in tetrahydrofuran (3 mL) was added. Under ice cooling, the mixture was stirred for 1 hour, and further stirred at room temperature. Insoluble materials were filtered off, the solvent was distilled off under reduced pressure, and the residue was isolated and purified by column chromatography on silica gel (hexane/ethyl acetate=2/1) to yield the title compound as a yellow powder (yield: 155 mg, 69.5%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07211577B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-333717e0bb544534a877158b4bc3d3a6
출처 메모uspto-grants-2007_05