反应 #1256776

ord-6a86a3b6305747439437ce8daa082353

反应方程式

Cc1ccc(NC(=O)NCc2cc(CN3CCN(C(=O)OC(C)(C)C)CC3)ccc2Cl)cn1
tert-butyl 4-(4-chloro-3-((3-(6-methylpyridin-3-yl)ureido)methyl)benzyl)piperazine-1-carboxylate
Cl
HCl
C1COCCO1
dioxane
Cc1ccc(NC(=O)NCc2cc(CN3CCNCC3)ccc2Cl)cn1.Cl.Cl.Cl
1-(2-chloro-5-(piperazin-1-ylmethyl)benzyl)-3-(6-methylpyridin-3-yl)urea trihydrochloride salt

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The solvents were removed

实验过程

The tert tert-butyl 4-(4-chloro-3-((3-(6-methylpyridin-3-yl)ureido)methyl)benzyl)piperazine-1-carboxylate from above (954 mg, 2.01 mmol) was dissolved in 40 mL of methanol and treated with 10 mL of 4N HCl in dioxane (40.2 mmol) with stirring for 16 h. The solvents were removed to afford 1.13 g of 1-(2-chloro-5-(piperazin-1-ylmethyl)benzyl)-3-(6-methylpyridin-3-yl)urea trihydrochloride salt as a white solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07825120B2uspto-grants-2010_11