beta-Aminobeta-ethoxyacrylic acid ethyl ester → HCID 20367323, compound
Reaction equation
C([O:3][C:4](=O)[CH:5]=[C:6]([NH2:10])OCC)C.[Cl:12][C:13]1[CH:21]=[CH:20][CH:19]=[C:18]([Cl:22])[C:14]=1[CH2:15][NH:16][NH2:17]>>[NH2:10][C:6]1[NH:17][N:16]([CH2:15][C:14]2[C:13]([Cl:12])=[CH:21][CH:20]=[CH:19][C:18]=2[Cl:22])[C:4](=[O:3])[CH:5]=1Participants
3
Procedure
35 g of β-amino-β-ethoxyacrylic acid ethyl ester and 38 g of 2,6-dichlorobenzylhydrazine when reacted as described in Example 45, yield 24 g of the compound identified above as colorless crystals, corresponding to 46% of theory, of melting point 225°.
Sources & evidence
- ORD record
- ord-273ced582c20452090a93734ff2eacaa
- Source dataset
- uspto-grants-1976_04
- Patent number
- US03950528
Reaction notes
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