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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 928263생성일: 2026년 10월 25일

4-Aminopyridine → 2-(5-Bromo-2-fluorophenyl)-4-(4-pyridylamino)pteridine

https://huagongshe.com/reaction/928263

반응식

참여 물질

역할이름HCID투입량
반응물4-AminopyridineHCID 1727—
반응물TriethylamineHCID 8471—
반응물PyBOPHCID 2724699—
반응물2-(5-Bromo-2-fluoro-phenyl)-3H-pteridin-4-oneHCID 136109958—
용매DichloromethaneHCID 6344—
생성물2-(5-Bromo-2-fluorophenyl)-4-(4-pyridylamino)pteridineHCID 1196221832.9%

반응 단계

Triethylamine (1.04 mL, 7.17 mmol) was added to a solution of 2-(5-bromo-2-fluoro-phenyl)pteridin-4-one 104 (800 mg, 2.49 mmol), 4-aminopyridine (469 mg, 4.98 mmol) and PyBOP (2.59 g, 4.98 mmol) in CH2Cl2. After 12 h, the reaction mixture was partitioned between CH2Cl2/Petroleum ether (2:1, 300 mL) and ice-cold 1N HCl (300 mL). The pH of the water phase was adjust to 12 with conc. NaOH and extracted with AcOEt, dried (Na2SO4) and evaporated. The residue was triturated in CH2Cl2/Petroleum ether (2:1, 15 mL), filtered off, and washed with ether. The product was purified by column chromatography (AcOEt/CH2Cl2/MeOH, 5:4:1) to give 325 mg of the title product 1 as a yellow powder (LCMS analysis).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09290502B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-e424538959524fd3a03095ac2cf1a4bf
출처 메모uspto-grants-2016_03