戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 16775作成日:2026年10月24日

Pyridine → Methyl 4-(4-methylpiperazine-1-carbonyl)benzoate

https://huagongshe.com/ja/reaction/16775

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Monomethyl terephthalateHCID 15513—
反応物1-MethylpiperazineHCID 53167—
反応物Oxalyl chlorideHCID 65578—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物Methyl 4-(4-methylpiperazine-1-carbonyl)benzoateHCID 1717822367.9%

反応手順

Oxalyl chloride (0.533 mL, 6.11 mmol) was added dropwise to a stirred suspension of 4-(methoxycarbonyl)benzoic acid (1 g, 5.55 mmol) in DCM (20 mL) under nitrogen. The resulting suspension was stirred at room temperature for 30 mins. DMF (0.05 mL) was added dropwise under nitrogen. The resulting suspension was stirred for 90 mins. A solution of 1-methylpiperazine (0.554 mL, 5.00 mmol) and pyridine (1.211 mL, 14.99 mmol) in DCM (15 mL) was added dropwise at 0° C., over a period of 60 mins under nitrogen. The resulting solution was stirred at room temperature for 3 h. The reaction mixture was evaporated to dryness to afford the crude product (1.791 g) as a dark orange solid. The solid was redissolved in DCM and washed with NaHCO3. The organic layer was evaporated to dryness to afford methyl 4-(4-methylpiperazine-1-carbonyl)benzoate (0.890 g, 61.1%) as an orange gum, which solidified on standing. Used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737149B2
出典データセットuspto-grants-2010_06
ORD IDord-fb35064d694440779fad2aeb07bf3334
出典メモuspto-grants-2010_06