Ethyl pyruvate → HCID 20565492, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[C:10]([NH2:15])=[CH:11][CH:12]=[CH:13][CH:14]=2)=[CH:4][CH:3]=1.[C:16](OCC)(=[O:20])[C:17]([CH3:19])=O>>[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:9]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[N:15]=[C:17]([CH3:19])[C:16]2=[O:20])=[CH:6][CH:7]=1Participants
3
Procedure
Preparation as in Example 1 but using N-(4-aminophenyl)benzene-1,2-diamine and ethyl pyruvate gave the title compound mp 269°-271° C.
Workup
- customPreparation as in Example 1
Sources & evidence
- ORD record
- ord-3422a2d9a81443398c4f2c465c0d66ca
- Source dataset
- uspto-grants-1981_10
- Patent number
- US04296114
Reaction notes
Loading…