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HRID 218080作成日:2026年10月25日

Formaldehyde → 4-[5-Methyl-2-(4-methylpiperazin-1-yl)-1,3-thiazol-4-yl]benzoic acid

https://huagongshe.com/reaction/218080

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物4-[4-(4-Carboxyphenyl)-5-methylthiazol-2-yl]-piperazine-1-carboxylic acidHCID 67195578—
反応物sodium;acetic acid;acetateHCID 178476574—
溶媒Hydrochloric AcidHCID 313—
溶媒1,4-DioxaneHCID 31275—
生成物4-[5-Methyl-2-(4-methylpiperazin-1-yl)-1,3-thiazol-4-yl]benzoic acidHCID 5980731995%

反応手順

4-[4-(4-Carboxyphenyl)-5-methylthiazol-2-yl]-piperazine-1-carboxylic acid tort-butyl ester (0.421 mmol) was dissolved in 4M HCl in 1,4-dioxane, and stirred at room temperature for 1 h. The solvent was then removed in vacuo, and the residue 4-(5-methyl-2-piperazin-1-yl-thiazol-4-yl)-benzoic acid was suspended in methanol (10 mL) and treated with AcOH/AcONa buffer (pH ˜5.5, 5 mL), and formaldehyde (0.547 mmol). The reaction mixture was stirred at room temperature for 1 h, then treated with NaCNBH3 (0.547 mmol) and stirred at room temperature overnight. The solvent was then removed under vacuum, and the residue was purified by column chromatography to afford the title compound (0.403 mmol, 95%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198283B2
出典データセットuspto-grants-2012_06
ORD IDord-cfdb7a612b9f4699bda65f09077a0aa7
出典メモuspto-grants-2012_06