反应 #543542

ord-a344e04afef74c478381fc0863cebf5f

反应方程式

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

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度the reaction mixture was refluxed for 3 h
  2. 2
    其他The white solid formed
  3. 3
    过滤was filtered
  4. 4
    洗涤the filter cake was washed with methylene chloride (50 mL)
  5. 5
    浓缩The combined filtrate and the washings were concentrated
  6. 6
    其他to give a thick oil which
  7. 7
    其他was dried under vacuum
  8. 8
    其他to afford a white solid
  9. 9
    其他This was used in the next step without further purification

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07186397B2uspto-grants-2007_03