반응 #706651

ord-e6fad21dceda42d2a790062eae7d9050

반응 방정식

Cc1nc2cccc3n(CCCCCN)c(=O)c1n23
3-methyl-1-[5-(amino)pentan-1-yl]-1,4,7b-triazacyclopent[cd]inden-2-one
CCN(CC)CC
triethylamine
CCOC(=O)C(F)(F)C(F)(F)F
pentafluoropropionic acid ethyl ester
Cc1nc2cccc3n(CCCCCNC(=O)C(F)(F)C(F)(F)F)c(=O)c1n23
desired compound
수율 50.5%
Cc1nc2cccc3n(CCCCCNC(=O)C(F)(F)C(F)(F)F)c(=O)c1n23
3-Methyl-1-[5-(pentafluoropropanoylamino)pentan-1-yl]-1,4,7b-triazacyclopent[cd]inden-2-one
수율 50.5%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGThe mixture was stirred for 4 hours at the same temperature
  2. 2
    workup.DISTILLATIONThe solvent was distilled off
  3. 3
    workup.ADDITIONTo the residue was added methylene chloride
  4. 4
    세척the mixture was washed with water
  5. 5
    건조dried over anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONThe solvent was distilled off
  7. 7
    기타the residue was purified by column chromatography (eluent: ethyl acetate)

실험 절차

To a solution of 2.58 g (10.0 mmol) of 3-methyl-1-[5-(amino)pentan-1-yl]-1,4,7b-triazacyclopent[cd]inden-2-one and 1.81 ml (13.0 mmol) of triethylamine in 100 ml of acetonitrile was added, while stirring at room temperature, 2.31 g (12.0 mmol) of pentafluoropropionic acid ethyl ester. The mixture was stirred for 4 hours at the same temperature. The solvent was distilled off. To the residue was added methylene chloride, and the mixture was washed with water, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by column chromatography (eluent: ethyl acetate) to afford 2.04 g of the desired compound (50.4%, a pale yellow solid).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05958942uspto-grants-1999_09