反应 #1909788

ord-0eafee68ac1d45dd8d917a72f88f747b

反应方程式

CN1CCN(CCO)CC1
2-(4-methylpiperazin-1-yl) ethanol
COC(=O)c1cc(Cl)c(O)c(Cl)c1O
3,5-dichloro-2,4-dihydroxybenzoic acid methyl ester
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
Cl
Hydrochloric acid
COC(=O)c1cc(Cl)c(OCCN2CCN(C)CC2)c(Cl)c1O
title compound
COC(=O)c1cc(Cl)c(OCCN2CCN(C)CC2)c(Cl)c1O
3,5-Dichloro-2-hydroxy-4-[2-(4-methylpiperazin-1-yl)-ethoxy]benzoic acid methyl ester

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

To a solution of 2-(4-methylpiperazin-1-yl) ethanol (14.42 g) and 3,5-dichloro-2,4-dihydroxybenzoic acid methyl ester (52.15 g) in chloroform (400 ml) were added triphenylphosphine (28.85 g) and azodicarboxylic acid diisopropyl (21.7 ml) at room temperature, and the mixture was stirred for 16 hours, 1N Hydrochloric acid (300 ml) was added to the reaction mixture for extraction to give a crude product of the title compound. Step 4) 3,5-Dichloro-2-hydroxy-4-[2-(4-methylpiperazin-1-yl)ethoxy]-benzoic acid (VII)

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE039088E1uspto-grants-2006_05