反応 #1980

ord-9c6f52c74e1f4a55a7103d040ea32d13

反応方程式

O=C(NC1CCN(Cc2ccccc2)C1)C(F)(F)F
compound
O=C(NC1CCN(Cc2ccccc2)C1)C(F)(F)F
1-benzyl-3-(2,2,2-trifluoroacetyl)aminopyrrolidine
[Al+3].[H-].[H-].[H-].[H-].[Li+]
LAH
FC(F)(F)CNC1CCN(Cc2ccccc2)C1
title compound
FC(F)(F)CNC1CCN(Cc2ccccc2)C1
1-benzyl-3-(2,2,2-trifluoroethyl)aminopyrrolidine

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGthe reaction was stirred at room temperature for 6 hours
  2. 2
    その他The reaction was quenched by sequential addition of 1.2 mL of water, 1.2 mL of 15% NaOH and 2.4 mL of water
  3. 3
    ろ過The mixture was filtered
  4. 4
    濃縮the filtrate was concentrated

実験手順

A 2.64 g sample of the compound from step 447a was added dropwise to a suspension of 1.11 g of LAH in ether stirred under N2 at 0° C. After one hour, the reaction was stirred at room temperature for 6 hours. The reaction was quenched by sequential addition of 1.2 mL of water, 1.2 mL of 15% NaOH and 2.4 mL of water. The mixture was filtered, and the filtrate was concentrated to give 2.39 of the title compound.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05726182uspto-grants-1998_03