Reaction equation
C([O:3][C:4](=O)[CH:5]=[C:6]([NH2:10])OCC)C.[N+:12]([C:15]1[CH:16]=[C:17]([CH:21]=[CH:22][CH:23]=1)[CH2:18][NH:19][NH2:20])([O-:14])=[O:13]>>[NH2:10][C:6]1[NH:20][N:19]([CH2:18][C:17]2[CH:21]=[CH:22][CH:23]=[C:15]([N+:12]([O-:14])=[O:13])[CH:16]=2)[C:4](=[O:3])[CH:5]=1Participants
3
Procedure
17.5 g of β-amino-β-ethoxyacrylic acid ethyl ester and 16.7 g of 3-nitrobenzylhydrazine, analogously to the procedure described in Example 1 yield 12.3 g of the compound identified above as yellow crystals of melting point 163°, corresponding to 52% of theory.
Sources & evidence
- ORD record
- ord-ceddf81bb8074af4936d1824326f91d0
- Source dataset
- uspto-grants-1977_12
- Patent number
- US04061653
Linked notes
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