反応 #51227

ord-7ceede82572049f485f3af7c071223a5

反応方程式

O=C(N[C@H]1CC[C@H](C(=O)N2Cc3ccc(CO)cc3C2)CC1)OCc1ccccc1
N-benzyloxycarbonyl-trans-4-[(5-hydroxylmethyl-2-isoindolinyl)carbonyl]cyclohexylamine
CCN(CC)CC
triethylamine
CS(=O)(=O)Cl
methanesulfonyl chloride
[Cl-]
chloride
N[C@H]1CC[C@H](C(=O)N2Cc3ccc(CN4CCOCC4)cc3C2)CC1
trans-4-[(5-morpholinomethyl-2-isoindolinyl)carbonyl]cyclohexylamine

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooling
  2. 2
    温度cooling for 1 hour
  3. 3
    抽出the mixture was extracted with ethyl acetate
  4. 4
    乾燥After the extract was dried over sodium sulfate
  5. 5
    その他the solvent was removed under reduced pressure
  6. 6
    workup.ADDITIONTo the residue were added 5 ml of dimethylformamide and 0.25 ml of morpholine
  7. 7
    workup.STIRRINGthe mixture was stirred at room temperature overnight
  8. 8
    workup.ADDITIONWater was added to the reaction mixture
  9. 9
    抽出the mixture was extracted with ethyl acetate
  10. 10
    乾燥After the extract was dried over anhydrous sodium sulfate
  11. 11
    その他the solvent was removed under reduced pressure
  12. 12
    その他The residue was purified by silica gel chromatography (solvent: chloroform-methanol=100:1)
  13. 13
    workup.ADDITIONThis compound was treated with palladium-carbon under hydrogen atmosphere

実験手順

0.15 ml of triethylamine and 0.07 ml of methanesulfonyl chloride were added to 10 ml of a tetrahydrofuranmethylene chloride suspension containing 0.31 g of N-benzyloxycarbonyl-trans-4-[(5-hydroxylmethyl-2-isoindolinyl)carbonyl]cyclohexylamine under ice-cooling, and the mixture was stirred under ice-cooling for 1 hour. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. After the extract was dried over sodium sulfate, the solvent was removed under reduced pressure. To the residue were added 5 ml of dimethylformamide and 0.25 ml of morpholine, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. After the extract was dried over anhydrous sodium sulfate, the solvent was removed under reduced pressure. The residue was purified by silica gel chromatography (solvent: chloroform-methanol=100:1). This compound was treated with palladium-carbon under hydrogen atmosphere to obtain trans-4-[(5-morpholinomethyl-2-isoindolinyl)carbonyl]cyclohexylamine (Reference Example 13-24 in Table 8).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06849622B2uspto-grants-2005_02