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HRID 989885生成日期:2026年10月23日

聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → HCID 23387834,化合物

https://huagongshe.com/zh-CN/reaction/989885

反应方程式

参与物

角色名称HCID投料
反应物聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
反应物1-(1,1-Dimethyl-1-butyloxycarbonyloxy)ethyl chlorideHCID 23449137—
反应物HCID 23669370HCID 23669370—
催化剂Silver iodideHCID 24563—
溶剂N,N-二甲基甲酰胺HCID 6228—
产物HCID 23387834HCID 2338783429.9%

反应步骤

A solution of 156.6 mg of 1-(1,1-dimethyl-1-butyloxycarbonyloxy)ethyl chloride in 2.0 ml of DMF was added to a suspension of 176.1 mg of silver iodide in 2.0 ml of DMF. The mixture was stirred in an argon atmosphere at room temperature for one hr. A solution of 200.0 mg of sodium(1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-(7-methylthio-imidazo[5,1-b]thiazol-2-yl)-1-carbapen-2-em-3-carboxylate in 1.0 ml of DMF was added thereto, followed by stirring for 3 hr. Water (10 ml) was added to the reaction solution to terminate the reaction. The system was extracted three times with 10 ml of ethyl acetate, followed by washing three times with 30 ml of semisaturated brine. The organic layer was dried over anhydrous magnesium sulfate and filtered. The residue was purified by chromatography on silica gel (chloroform:methanol=20:1) to give 82.3 mg of the title compound.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US06458780B1
来源数据集uspto-grants-2002_10
ORD IDord-675901b43e19495ab0dd9350190c3749
来源说明uspto-grants-2002_10