Реакция #2446086

ord-5925de3b7db240618f509d1a178d0a54

Уравнение реакции

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

Растворители

Условия реакции

Температура
50°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe reaction mixture heated at 60° C. for another 24 hours
  2. 2
    ФильтрацияThe reaction mixture was filtered
  3. 3
    Промывкаwashed 5% methanol-DCM
  4. 4
    КонцентрированиеThe filtrate was concentrated
  5. 5
    Другоеthe crude material was purified by Combiflash® chromatography
  6. 6
    Промывкаeluting with 6-7% methanol/DCM

Методика

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)

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08685418B2uspto-grants-2014_04