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HRID 130337作成日:2026年10月25日

4-Bromopyridinium chloride → Pyridazine, 3-phenyl-5-(4-pyridinyl)-

https://huagongshe.com/reaction/130337

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromopyridinium chlorideHCID 88100—
反応物Pyridazine, 3-phenyl-5-(tributylstannyl)-HCID 11729979—
触媒HCID 178418397HCID 178418397—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
溶媒Ammonium ChlorideHCID 25517—
生成物Pyridazine, 3-phenyl-5-(4-pyridinyl)-HCID 1019855369.4%

反応条件

温度150 °C

反応手順

3-Phenyl-5-(tri-n-butylstannyl)pyridazine (110 mg, 0.247 mmol), 4-bromopyridine hydrochloride (72 mg, 0.370 mmol) and Pd(PPh3)4 (10 mg) in THF (2 ml) were combined and heated to 150° C. for 60 min in a Smith Synthesiser microwave reactor (Personal Chemistry, Uppsala, Sweden). The reaction was diluted with CH2Cl2 (6 ml) and NH4Cl (2 ml) then poured into PTFE (5 μM) fritted syringe barrels. The organic phase was collected and concentrated while loading onto silica. The compound was purified by dry flash column chromatography to give the title compound as a white solid (40 mg). δH (400 MHz, d6 DMSO) 7.36-7.63 (3H, m), 8.10 (2H, dd, J 1.8 and 4.5), 8.32 (2H, m), 8.62 (1H, d, J 2.0), 8.80-8.82 (2H, dd, J 1.8 and 4.5), 9.71 (2H, d, J 2.0); m/z (ES+) 234 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381725B2
出典データセットuspto-grants-2008_06
ORD IDord-6ab7387de01244b79f01f726fa6820c7
出典メモuspto-grants-2008_06