HCID 21701834, compound → HCID 59370069, compound

HRID 1924615Notes

Reaction equation

HRID 1924615 reaction equation
CN(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][C:17]([O:20][C:21]([F:24])([F:23])[F:22])=[CH:16][CH:15]=2)[N:8]=1)=O.[NH:26]([C:28]1[CH:29]=[C:30]([S:34]([N:37]([CH3:39])[CH3:38])(=[O:36])=[O:35])[CH:31]=[CH:32][CH:33]=1)[NH2:27]>>[CH3:38][N:37]([CH3:39])[S:34]([C:30]1[CH:31]=[CH:32][CH:33]=[C:28]([N:26]2[C:5]([C:7]3[C:12](=[O:13])[CH:11]=[CH:10][N:9]([C:14]4[CH:15]=[CH:16][C:17]([O:20][C:21]([F:23])([F:24])[F:22])=[CH:18][CH:19]=4)[N:8]=3)=[CH:4][CH:3]=[N:27]2)[CH:29]=1)(=[O:36])=[O:35]

Participants

3

Reactant 2

HCID 21701834HCID 21701834, compoundHCID 593700343-((E)-3-Dimethylamino-acryloyl)-1-(4-trifluoromethoxy-phenyl)-1H-pyridazin-4-one

Product 1

HCID 59370069HCID 59370069, compound

Procedure

The product was obtained starting from 3-((E)-3-Dimethylamino-acryloyl)-1-(4-trifluoromethoxy-phenyl)-1H-pyridazin-4-one (A-8) and 3-hydrazino-N,N-dimethyl-benzenesulfonamide according to the method described for example 91.

Workup

  1. customThe product was obtained

Sources & evidence

ORD record
ord-3aae5c652d114c0e9bcc9ecb4333f8e7
Source dataset
uspto-grants-2012_05
Patent number
US08178538B2

Reaction notes

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