反应 #2446086

ord-5925de3b7db240618f509d1a178d0a54

反应方程式

CCI
Ethyl iodide
CC(CNC1CCCCC1)OC(=O)c1ccccc1
benzoic acid 2-cyclohexylamino-1-methyl-ethyl ester
O=C([O-])[O-].[K+].[K+]
K2CO3
CCI
ethyl iodide
CCN(CC(C)OC(=O)c1ccccc1)C1CCCCC1
1-(cyclohexyl(ethyl)amino)propan-2-yl benzoate

溶剂

反应条件

温度
50°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度the reaction mixture heated at 60° C. for another 24 hours
  2. 2
    过滤The reaction mixture was filtered
  3. 3
    洗涤washed 5% methanol-DCM
  4. 4
    浓缩The filtrate was concentrated
  5. 5
    其他the crude material was purified by Combiflash® chromatography
  6. 6
    洗涤eluting with 6-7% methanol/DCM

实验过程

To a stirred solution of benzoic acid 2-cyclohexylamino-1-methyl-ethyl ester (1.0 g, 3.8 mmol) in DCE (20 mL) were added successively K2CO3 (2.11 g, 15.2 mmol) and ethyl iodide (1.8 mL, 22 mmol). The resulting mixture was heated at 50° C. for 16 hours in a sealed tube. Ethyl iodide (1.8 mL) was again added and the reaction mixture heated at 60° C. for another 24 hours. The reaction mixture was filtered and washed 5% methanol-DCM. The filtrate was concentrated and the crude material was purified by Combiflash® chromatography eluting with 6-7% methanol/DCM to provide 1-(cyclohexyl(ethyl)amino)propan-2-yl benzoate. Yield: 1.04 g (94.70%). 1H NMR (DMSO-d6) δ 7.95 (d, J=7 Hz, 2 H), 7.64 (t, J=7 Hz, 1 H), 7.52 (t, J=8 Hz, 2 H), 5.08-5.04 (m, 1 H), 2.68-2.62 (m, 1 H), 2.55-2.40 (m, 4 H), 1.70-1.53 (m, 5 H), 1.26 (d, J=6 Hz, 3 H), 1.19-1.07 (m, 5 H), 0.93 (t, J=7 Hz, 3 H). LCMS: m/z=290.4 [M+H], RT=3.93 min, (Column: Y, Program: P1)

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08685418B2uspto-grants-2014_04