HRID61483

反应详情

EQUATION

反应方程式

HRID 61483 的结构方程式

PROCEDURE

实验过程

To a stirred mixture of (3R,4S)-piperidine-1,3,4-tricarboxylic acid 1-benzyl ester 3-methyl ester (0.554 g, 0.00172 mol) in N,N-dimethylformamide (8.500 mL, 0.1098 mol) was added 3-methyl-4-piperazin-1-ylbenzonitrile dihydrochloride (0.6146 g, 0.002241 mol), (benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate (1.017 g, 0.001896 mol), and, N,N-diisopropylethylamine (1.509 mL, 0.008620 mol). The reaction mixture was stirred overnight at room temp. Reaction quenched with KH2PO4 (sat solution). Layers separated and aq layer extracted with ethyl acetate 3×. Organic layers were washed with brine and dried over magnesium sulfate. Filtered and concentrated. The residue was purified by Combiflash with 40-70% EtOAc/Hex to give the product (75% in yield). MS (ESI): (M+H)+=505.

WORKUP

后处理

  1. customReaction
  2. customquenched with KH2PO4 (sat solution)
  3. customLayers separated
  4. extractionaq layer extracted with ethyl acetate 3×
  5. washOrganic layers were washed with brine
  6. dry with materialdried over magnesium sulfate
  7. filtrationFiltered
  8. concentrationconcentrated
  9. customThe residue was purified by Combiflash with 40-70% EtOAc/Hex
  10. customto give
  11. customthe product (75% in yield)