返回
化工社化工社化学信息打印报告 · 仅供科研参考
HRID 251663生成日期:2026年10月24日

三乙胺 → 6-(5-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamido)-hexanoic acid methyl ester

https://huagongshe.com/zh-CN/reaction/251663

反应方程式

参与物

角色名称HCID投料
反应物三乙胺HCID 8471—
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6-氨基己酸甲酯盐酸盐HCID 11499324—
反应物5-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acidHCID 136387942—
反应物HCID 178418300HCID 178418300—
溶剂N,N-二甲基甲酰胺HCID 6228—
溶剂Sodium chloride; waterHCID 57417360—
产物6-(5-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxamido)-hexanoic acid methyl esterHCID 13638795063%

反应步骤

5-(((5-fluoro-2-oxoindolin-3-ylidene)hydrazono)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (328 mg, 1 mmol) and 8 ml of DMF were stirred at room temperature while 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (394 mg, 2 mmol), hydroxybenzo-triazole (162 mg, 1.2 mmol), triethylamine (404 mg, 4 mmol) and 6-aminocaproic acid methyl ester hydrochloride (219 mg, 1.2 mmol) were added. The mixture was stirred for 24 hours at room temperature. The mixture was diluted with 400 mL of brine. The solids were collected by vacuum filtration, washed with water and dried under vacuum to give the title compound (287 mg, 63% yield) as a red solid. LC-MS (m/z) 456 (M+1).

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US07863315B2
来源数据集uspto-grants-2011_01
ORD IDord-bce9baaea7a94ebbbb536abff35ba017
来源说明uspto-grants-2011_01