HCID 12138644, compound → HCID 59369986, compound

HRID 1924704Notes

Reaction equation

HRID 1924704 reaction equation
C[N:2](C)/[CH:3]=[CH:4]/[C:5]([C:7]1[C:12](=[O:13])[CH:11]=[CH:10][N:9]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[N:8]=1)=O.[Cl:21][C:22]1[C:31]2[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=2)[C:25]([NH:32]N)=[CH:24][CH:23]=1>>[Cl:21][C:22]1[C:31]2[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=2)[C:25]([N:32]2[C:5]([C:7]3[C:12](=[O:13])[CH:11]=[CH:10][N:9]([C:14]4[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=4)[N:8]=3)=[CH:4][CH:3]=[N:2]2)=[CH:24][CH:23]=1

Participants

3

Reactant 2

HCID 12138644HCID 12138644, compoundHCID 12742246(E)-3-(3-(Dimethylamino)acryloyl)-1-phenylpyridazin-4(1H)-one

Product 1

HCID 59369986HCID 59369986, compound

Procedure

The product was obtained starting from 3-((E)-3-Dimethylamino-acryloyl)-1-phenyl-1H-pyridazin-4-one (A-1) and (4-chloro-naphthalen-1-yl)-hydrazine according to the method described for example 1. MS: M=399.1 (M+H)+

Workup

  1. customThe product was obtained

Sources & evidence

ORD record
ord-09205e0c4e354e5f81559ef802668037
Source dataset
uspto-grants-2012_05
Patent number
US08178538B2

Reaction notes

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