Ethyl pyruvate → HCID 20565479, compound
Reaction equation
[C:1]([CH2:4][C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]2[C:13]([NH2:18])=[CH:14][CH:15]=[CH:16][CH:17]=2)=[CH:7][CH:6]=1)([OH:3])=[O:2].[C:19](OCC)(=[O:23])[C:20]([CH3:22])=O>>[C:1]([CH2:4][C:5]1[CH:6]=[CH:7][C:8]([N:11]2[C:12]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[N:18]=[C:20]([CH3:22])[C:19]2=[O:23])=[CH:9][CH:10]=1)([OH:3])=[O:2]Participants
3
Procedure
Preparation as in Example 1 but using N-(4-carboxymethylphenyl)benzene-1,2-diamine and ethyl pyruvate gave the title compound mp 179°-181.5° C.
Workup
- customPreparation as in Example 1
Sources & evidence
- ORD record
- ord-d9ee94937260416780f4f2e086502979
- Source dataset
- uspto-grants-1981_10
- Patent number
- US04296114
Reaction notes
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