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HRID 1092064作成日:2026年10月27日

Trimethylsilyldiazomethane → Methyl 4-((4-methylpiperazin-1-yl)methyl)benzoate

https://huagongshe.com/reaction/1092064

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylsilyldiazomethaneHCID 167693—
反応物4-(4-Methyl-1-piperazinylmethyl)benzoic acidHCID 4769782—
溶媒MethanolHCID 887—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物Methyl 4-((4-methylpiperazin-1-yl)methyl)benzoateHCID 78222244.2%

反応手順

A solution of (trimethylsilyl)diazomethane ((0.611 mL, 3.84 mmol) 2.0M in diethyl ether) was added dropwise to a stirred suspension of 4-((4-methylpiperazin-1-yl)methyl)benzoic acid (0.75 g, 3.20 mmol) in toluene (21 mL) and methanol (7 mL) over a period of 10 mins under nitrogen. The resulting suspension was stirred at room temperature for 3 h. A further aliquot of (trimethylsilyl)diazomethane (1.222 mL, 7.68 mmol) was added dropwise and the solution was stirred at room temperature for a further 18 h. The reaction mixture was evaporated to dryness to afford the crude product (0.723 g) as a white solid. This was taken up in DCM and the insolubles were filtered off. The filtrate was evaporated to dryness to afford the crude product. This was taken up in DCM again and more insolubles were filtered off to afford methyl 4-((4-methylpiperazin-1-yl)methyl)benzoate (0.351 g, 44.2%), which was used without purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08129391B2
出典データセットuspto-grants-2012_03
ORD IDord-4d95eaf64740474096573688ff61119a
出典メモuspto-grants-2012_03