HCID 2756287, compound → HCID 178467133, compound

HRID 2372204Notes

Reaction equation

HRID 2372204 reaction equation
[C:1]([C:4]1[CH:5]=[N:6][C:7]2[C:12]([C:13]=1[C:14]([OH:16])=O)=[CH:11][CH:10]=[CH:9][CH:8]=2)(=[O:3])[CH3:2].[Cl:17][C:18]1[CH:19]=[C:20]([NH:24][C:25](=[O:28])[NH:26][NH2:27])[CH:21]=[CH:22][CH:23]=1>>[Cl:17][C:18]1[CH:19]=[C:20]([NH:24][C:25](=[O:28])[NH:26][N:27]=[C:14]([C:13]2[C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[N:6]=[CH:5][C:4]=2[C:1](=[O:3])[CH3:2])[OH:16])[CH:21]=[CH:22][CH:23]=1

Participants

3

Reactant 2

HCID 2756287HCID 2756287, compoundHCID 2757857Hydrazinecarboxamide, N-(3-chlorophenyl)-

Product 1

HCID 178467133HCID 178467133, compound

Procedure

In the same manner, 3-acetyl-4-quinolinecarboxylic acid is reacted with 4-(3-chlorophenyl)semicarbazide to give 3-acetyl-4-quinolinecarboxylic acid 4-(3-chlorophenyl)semicarbazone, m.p. 229° (compound 104).

Sources & evidence

ORD record
ord-cae5223004f842b09bd23c673ca5f7a2
Source dataset
uspto-grants-1992_03
Patent number
US05098466

Reaction notes

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