Hydrazine hydrate (1:1) → HCID 21488581, compound

HRID 1974063Notes

Reaction equation

HRID 1974063 reaction equation
Cl[C:2]1[CH:11]=[C:10]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[Cl:18])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:19]([O-:21])=[O:20])[CH:8]=2)[N:3]=1.O.[NH2:23][NH2:24]>>[N+:19]([C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([NH:23][NH2:24])[CH:11]=[C:10]2[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[Cl:18])([O-:21])=[O:20]

Participants

3

Reactant 2

HCID 24654Hydrazine hydrate (1:1)HCID 21488634HCID 21488634, compound

Product 1

HCID 21488581HCID 21488581, compound

Procedure

In the manner given in Example 1, 2-chloro-6-nitro-4-(o-chlorophenyl)quinoline is reacted at reflux with hydrazine hydrate to give 6-nitro-4-(o-chlorophenyl)-2-hydrazinoquinoline

Workup

  1. customis reacted

Sources & evidence

ORD record
ord-2c26677e584e4eb0aecdcc4bd461e7d1
Source dataset
uspto-grants-1976_12
Patent number
US04000151

Reaction notes

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