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HRID 517543生成日期:2026年10月26日

1-羟基苯并三唑(HOBT) → N-(2-hydroxy-1-phenylethyl)-4-methyl-5-(3-(4-methylpiperazin-1-yl)benzyl)thiazole-2-carboxamide

https://huagongshe.com/reaction/517543

反应方程式

参与物

角色名称HCID投料
反应物1-羟基苯并三唑(HOBT)HCID 75771—
反应物D-苯甘氨醇HCID 92466—
反应物1-乙基-(3-二甲基氨基丙基)碳酰二亚胺盐酸盐HCID 2723939—
反应物4-Methyl-5-(3-(4-methylpiperazin-1-yl)benzyl)thiazole-2-carboxylic acidHCID 86711482—
溶剂聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
溶剂N,N-二甲基甲酰胺HCID 6228—
产物N-(2-hydroxy-1-phenylethyl)-4-methyl-5-(3-(4-methylpiperazin-1-yl)benzyl)thiazole-2-carboxamideHCID 8671148348.1%

反应条件

温度50 °C

反应步骤

To a mixture of 4-methyl-5-(3-(4-methylpiperazin-1-yl)benzyl)thiazole-2-carboxylic acid (200 mg, 0.6 mmol), 2-amino-2-phenylethanol (99 mg, 0.7 mmol) and TEA (0.3 mL, 1.8 mmol) in DMF (2 mL), EDCI.HCl (175 mg, 0.9 mmol) and HOBT (95 mg, 0.7 mmol) were added. The mixture was stirred at 50° C. overnight, then cooled to RT, diluted with H2O (50 mL) and extracted with DCM/MeOH (10/1, 4×30 mL). The combined organic layers were washed with a saturated aqueous solution of LiCl (3×20 mL) and brine (20 mL), dried over Na2SO4, filtered, and concentrated to afford the crude product, which was purified by Combiflash reverse phase chromatography (50%˜60% MeCN/H2O containing 10 mM NH4HCO3) to afford N-(2-hydroxy-1-phenylethyl)-4-methyl-5-(3-(4-methylpiperazin-1-yl)benzyl)thiazole-2-carboxamide as a colorless oil (130 mg, 48%). MS (ES+) C25H30N4O2S requires: 450, found: 451 [M+H]+.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US09115120B2
来源数据集uspto-grants-2015_08
ORD IDord-044858c0874c4bf38b404f776ddc9243
来源说明uspto-grants-2015_08