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HRID 1093959作成日:2026年10月25日

Cyclohexylamine → 5-bromo-N-cyclohexylimidazo[1,2-a]pyrazin-8-amine

https://huagongshe.com/reaction/1093959

反応式

関与物質

役割名称HCID仕込み量
反応物CyclohexylamineHCID 7965—
反応物DiisopropylethylamineHCID 81531—
反応物5,8-Dibromoimidazo[1,2-a]pyrazineHCID 53485949—
溶媒IsopropanolHCID 3776—
生成物5-bromo-N-cyclohexylimidazo[1,2-a]pyrazin-8-amineHCID 5769948769.2%

反応条件

温度90 °C

反応手順

Intermediate 2 (5,8-Dibromoimidazo[1,2-a]pyrazine, 200 mg, 0.72 mmol), cyclohexylamine (86 mg, 0.86 mmol) and di-isopropylethylamine (140 mg, 0.74 mmol) are suspended in iso-propanol (5 ml). The mixture is stirred at 90° C. for 18 h. The solvent is evaporated in vacuo and the residue dissolved in dichloromethane (5 mL). The organic layer is washed with saturated NaHCO3(aq) (10 ml), H2O (10 ml) and brine (10 mL). The organic layer is dried (MgSO4) and evaporated in vacuo. The oily residue is purified by column chromatography, eluting with 5:1 hexane:ethyl acetate to give a brown oil (147 mg, 69%). 1H-NMR (400 MHz, d6-DMSO) =1.22-1.29 (m, 1H), 1.32-1.49 (m, 4H), 1.64 (d, 1H, J=15.2 Hz), 1.77 (d, 2H, J=12.8 Hz), 1.92 (d, 2H, J=15.2 Hz), 3.97-4.01 (1H, m), 7.33 (d, 1H, J=8.4 Hz), 7.48 (s, 1H), 7.63 (s, 1H), 7.92 (s, 1H). LCMS: Rt 3.83 min (99.8%), m/z (APCI) 295 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08133895B2
出典データセットuspto-grants-2012_03
ORD IDord-3862a0fe5efe45a5913d9c1229af7dc2
出典メモuspto-grants-2012_03