Ethyl pyruvate → HCID 20565467, compound

HRID 848466Notes

Reaction equation

HRID 848466 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[C:10]([NH2:16])=[CH:11][CH:12]=[C:13]([CH3:15])[CH:14]=2)=[CH:4][CH:3]=1.[C:17](OCC)(=[O:21])[C:18]([CH3:20])=O>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:9]3[C:10](=[CH:11][CH:12]=[C:13]([CH3:15])[CH:14]=3)[N:16]=[C:18]([CH3:20])[C:17]2=[O:21])=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 12041Ethyl pyruvateHCID 20565473HCID 20565473, compound

Product 1

HCID 20565467HCID 20565467, compound

Procedure

Preparation as in Example 1 but using N-(4-chlorophenyl)-5-methylbenzene-1,2-diamine and ethyl pyruvate gave the title compound mp 144°-145° C.

Workup

  1. customPreparation as in Example 1

Sources & evidence

ORD record
ord-7706f974b7284f9985507fab8c7b9653
Source dataset
uspto-grants-1981_10
Patent number
US04296114

Reaction notes

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