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HRID 1695209作成日:2026年10月25日

Potassium Iodide → 1040718-40-8

https://huagongshe.com/reaction/1695209

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物N-AcetylhomopiperazineHCID 4186202—
反応物5-bromo-N-(5-(4-methoxyphenyl)-1H-pyrazol-3-yl)pentanamideHCID 57780044—
反応物HCID 178506555HCID 178506555—
溶媒AcetoneHCID 180—
生成物1040718-40-8HCID 24860582—

反応条件

温度27.5 °C

反応手順

To a cylindrical, jacketed 3 L reactor equipped with nitrogen inerting, agitator, condenser/distillation head, and temperature control, 5-bromo-pentanoic acid [5-(4-methoxy-phenyl)-1H-pyrazol-3-yl]amide (0.15 kg, 0.426 mol), potassium carbonate (0.059 kg, 0.426 mol), potassium iodide (0.071 kg, 0.426 mol), and acetone (1.18 kg, 1.5 L) were added (at 20° C.) to form a white mixture. The mixture was stirred (235 rpm) at 25-30° C. for a minimum of 15 min. N-acetylhomopiperazine (0.062 kg, 0.057 L, 0.434 mol) was added via addition funnel to the reactor over a minimum of 45 min., maintaining the temperature in the range of 25-30° C. The addition funnel was rinsed with 0.05 L acetone. A white mixture persisted. The mixture was stirred (235 rpm) in the range of 25-30° C. for a minimum of 16 h, forming a white/yellow mixture. The reaction progress was monitored by HPLC and was considered complete when there was ≦2% of the starting material (bromopyrazole) and ≦2% of the iodopyrazole present.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08163729B2
出典データセットuspto-grants-2012_04
ORD IDord-00121884c5954f27a6912dcc169de615
出典メモuspto-grants-2012_04