Reacción #543542

ord-a344e04afef74c478381fc0863cebf5f

Ecuación de reacción

CC(=NO)C(C)(C)NOCCNC(C)(C)C(CCN1C(=O)c2ccccc2C1=O)=NO
12-phthalimido-3,3,9,9-tetramethyl-5-oxa-4,8-diaza-2,10-dodecane dione dioxime
CC(=NO)C(C)(C)NOCCNC(C)(C)C(CCN1C(=O)c2ccccc2C1=O)=NO
12-Phthalimido-3,3,9,9-tetramethyl-5-oxa-4,8-diaza-2,10-dodecanedione dioxime
NN
hydrazine
CC(=NO)C(C)(C)NOCCNC(C)(C)C(CCN)=NO
12-Amino-3,3,9,9-tetramethyl-5-oxa-4,8-diaza-2,10-dodecanedione dioxime

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe reaction mixture was refluxed for 3 h
  2. 2
    OtroThe white solid formed
  3. 3
    Filtraciónwas filtered
  4. 4
    Lavadothe filter cake was washed with methylene chloride (50 mL)
  5. 5
    ConcentraciónThe combined filtrate and the washings were concentrated
  6. 6
    Otroto give a thick oil which
  7. 7
    Otrowas dried under vacuum
  8. 8
    Otroto afford a white solid
  9. 9
    OtroThis was used in the next step without further purification

Procedimiento

To a solution of 12-phthalimido-3,3,9,9-tetramethyl-5-oxa-4,8-diaza-2,10-dodecane dione dioxime (52a) (2.0 g, 4.6 mmol) in methylene chloride (100 mL) was added hydrazine (0.3 mL, 9.3 mmol) and the reaction mixture was refluxed for 3 h. The white solid formed was filtered and the filter cake was washed with methylene chloride (50 mL). The combined filtrate and the washings were concentrated to give a thick oil which was dried under vacuum to afford a white solid. Yield: 1.2 g (82%). MS: (M+H)+=304.1. This was used in the next step without further purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07186397B2uspto-grants-2007_03