反应 #1702152

ord-23e6ee683fec44ed87357cb874b0ce48

反应方程式

O=C([O-])[O-].[Na+].[Na+]
Na2CO3
COc1ccc(Br)c(CNc2nc(Nc3cccc(CCCO)c3)ncc2Cl)c1
3-[3-({4-[(2-bromo-5-methoxybenzyl)amino]-5-chloropyrimidin-2-yl}amino)phenyl]propan-1-ol
BrB(Br)Br
boron tribromide
Oc1ccc(Br)c(CNc2nc(Nc3cccc(CCCBr)c3)ncc2Cl)c1
desired product
收率 91.0%
Oc1ccc(Br)c(CNc2nc(Nc3cccc(CCCBr)c3)ncc2Cl)c1
4-Bromo-3-{[(2-{[3-(3-bromopropyl)phenyl]amino}-5-chloropyrimidin-4-yl)amino]methyl}phenol
收率 91.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added
  2. 2
    过滤The mixture was filtered
  3. 3
    其他the solid collected
  4. 4
    其他was triturated with EtOAc
  5. 5
    洗涤by washing with cold water

实验过程

To a solution of 3-[3-({4-[(2-bromo-5-methoxybenzyl)amino]-5-chloropyrimidin-2-yl}amino)phenyl]propan-1-ol (3.0 g, 6.3 mmol) in methylene chloride (40 mL) was added slowly a solution of boron tribromide in methylene chloride (31 mL, 31 mmol, 1.0 M) at 0° C. The mixture was allowed to warm up to rt and stirred over the weekend. The resultant mixture was cooled in dry ice when Na2CO3 (saturated aqueous solution) was added. The mixture was filtered and the solid collected was triturated with EtOAc, followed by washing with cold water to give the desired product (3.0 grams, 91%) as an off-white powder. LCMS for C20H19Br2ClN4O (M+H)+: m/z=524.8, 526.8, 528.7.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08765727B2uspto-grants-2014_07