HRID1254384

反应详情

EQUATION

反应方程式

HRID 1254384 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of mono-methyl isophthalate (0.3230 g, 1.79 mmol, 1.0 equiv), 2-(trimethylsilyl)ethyl (S)-2-amino-3-cyclohexylpropylmethylcarbamate (0.5573 g, 1.77 mmol, 0.99 equiv), EDC (0.6200 g, 1.8 equiv), HOBT (0.4035 g, 1.66 equiv), and DIEA (3.6 mL, 11 equiv) in CH2Cl2 (20 mL) was stirred at rt for 18 h. The reaction mixture was quenched with 10% aq Na2CO3, extracted with CH2Cl2 and dried over Na2SO4. After the solvent was removed, the crude (S)-methyl 3-(1-cyclohexyl-3-(N-methyl-N-(2-(trimethylsilyl)ethoxycarbonyl)amino)propan-2-ylcarbamoyl)benzoate (1.397 g) was used in the next step without further purification. LC-MS (3 min) to=2.29 min, m/z 499 (M+Na+), 449, 359.

WORKUP

后处理

  1. customThe reaction mixture was quenched with 10% aq Na2CO3
  2. extractionextracted with CH2Cl2
  3. dry with materialdried over Na2SO4
  4. customAfter the solvent was removed
  5. customthe crude (S)-methyl 3-(1-cyclohexyl-3-(N-methyl-N-(2-(trimethylsilyl)ethoxycarbonyl)amino)propan-2-ylcarbamoyl)benzoate (1.397 g) was used in the next step without further purification
  6. customLC-MS (3 min)
  7. customto=2.29 min, m/z 499 (M+Na+), 449, 359