HCID 5704109, compound → HCID 59370000, compound

HRID 1924711Notes

Reaction equation

HRID 1924711 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:13]=[CH:12][C:11](=[O:14])[C:10]([C:15](=O)/[CH:16]=[CH:17]/[N:18](C)C)=[N:9]2)=[CH:4][CH:3]=1.[Cl:22][C:23]1[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[C:26]([NH:33]N)=[CH:25][CH:24]=1>>[Cl:22][C:23]1[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[C:26]([N:33]2[C:15]([C:10]3[C:11](=[O:14])[CH:12]=[CH:13][N:8]([C:5]4[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][CH:6]=4)[N:9]=3)=[CH:16][CH:17]=[N:18]2)=[CH:25][CH:24]=1

Participants

3

Reactant 2

HCID 5704109HCID 5704109, compoundHCID 12138644HCID 12138644, compound

Product 1

HCID 59370000HCID 59370000, compound

Procedure

The product was obtained starting from 1-(4-Chloro-phenyl)-3-((E)-3-dimethylamino-acryloyl)-1H-pyridazin-4-one (A-24) and (4-chloro-naphthalen-1-yl)-hydrazine according to the method described for example 1. MS: M=433.1 (M+H)+

Workup

  1. customThe product was obtained

Sources & evidence

ORD record
ord-f130d69631184e31a385e0f34b976dab
Source dataset
uspto-grants-2012_05
Patent number
US08178538B2

Reaction notes

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