反应 #1135837

ord-ab4a5b1697ae44abb85e3b081d3fea93

反应方程式

[K+].[OH-]
KOH
COC(=O)CCCCCCc1nc2ccc(-c3ccccc3)cc2[nH]1
methyl 7-(6-phenyl-1H-benzo[d]imidazol-2-yl)heptanoate
NO
hydroxylamine
O=C(CCCCCCc1nc2ccc(-c3ccccc3)cc2[nH]1)NO
N-hydroxy-7-(6-phenyl-1H-benzo[d]imidazol-2-yl)heptanamide
收率 53.3%

溶剂

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩briefly concentrated
  2. 2
    workup.ADDITIONby adding 1 N HCl solution until pH was 7
  3. 3
    过滤The white precipitate was collected by filtration
  4. 4
    其他purified by biotage column chromatography

实验过程

To a solution of methyl 7-(6-phenyl-1H-benzo[d]imidazol-2-yl)heptanoate (50 mg, 0.15 mmol) in THF at 0° C. was added 50% hydroxylamine solution (0.10 mL, 1.5 mmol). To this was added KOH (0.45 mL, 1M in MeOH, 0.45 mmol) dropwise. The reaction was stirred at 0° C. for 2 hr, briefly concentrated and neutralized by adding 1 N HCl solution until pH was 7. The white precipitate was collected by filtration and purified by biotage column chromatography to give N-hydroxy-7-(6-phenyl-1H-benzo[d]imidazol-2-yl)heptanamide 18 (27 mg). MS (M+1=338)

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09381196B2uspto-grants-2016_07