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HRID 928263作成日:2026年10月25日

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

https://huagongshe.com/reaction/928263

反応式

関与物質

役割名称HCID仕込み量
反応物4-AminopyridineHCID 1727—
反応物TriethylamineHCID 8471—
反応物PyBOPHCID 2724699—
反応物2-(5-Bromo-2-fluoro-phenyl)-3H-pteridin-4-oneHCID 136109958—
溶媒DichloromethaneHCID 6344—
生成物2-(5-Bromo-2-fluorophenyl)-4-(4-pyridylamino)pteridineHCID 1196221832.9%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09290502B2
出典データセットuspto-grants-2016_03
ORD IDord-e424538959524fd3a03095ac2cf1a4bf
出典メモuspto-grants-2016_03