반응 #45872

ord-86b2c1cb486d4551bdda45bf80d26985

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the solvent was evaporated away under reduced pressure
  2. 2
    workup.ADDITIONEther was added to the residue
  3. 3
    농축this was concentrated under reduced pressure
  4. 4
    workup.ADDITIONEther was added to the residue
  5. 5
    기타followed by sonication
  6. 6
    기타the solvent was removed with a pipette
  7. 7
    기타The residue was dried at 60° C. under reduced pressure for 2 hours

실험 절차

2-Cyclopropyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-6-(3-hydroxycyclopent-1-enyl)-5-methyl-1,3-benzoxazole-4-carbonitrile (I-306) (83 mg, 0.21 mmol) was dissolved in ethanol (0.85 ml) and diethyl ether (1.7 ml), and at room temperature, 1 M hydrochloric acid/ethanol solution (222 μl, 0.22 mmol) was added. After stirring at the same temperature for 4 hours, the solvent was evaporated away under reduced pressure. Ether was added to the residue, and this was concentrated under reduced pressure. This operation was repeated once again. Ether was added to the residue, followed by sonication, and the solvent was removed with a pipette. The residue was dried at 60° C. under reduced pressure for 2 hours to obtain the entitled compound (62 g, 65%) as a brown solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07737166B2uspto-grants-2010_06