2,4-Dichlorobenzoic Acid → HCID 86716398, compound

HRID 512345Notes

Reaction equation

HRID 512345 reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[C:12]1([CH:18]([C:21]2[CH:26]=[CH:25][N:24]=[N:23][CH:22]=2)[CH2:19][NH2:20])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[CH:8]=[CH:7][C:3]=1[C:4]([NH:20][CH2:19][CH:18]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:21]1[CH:26]=[CH:25][N:24]=[N:23][CH:22]=1)=[O:6]

Participants

3

Reactant 2

HCID 57872,4-Dichlorobenzoic AcidHCID 86716225HCID 86716225, compound

Product 1

HCID 86716398HCID 86716398, compound

Procedure

From 2,4-dichlorobenzoic acid and 2-phenyl-2-(pridazin-4-yl)ethanamine. LCMS (MH+): m/z=372.1, tR (minutes, Method G)=2.09

Sources & evidence

ORD record
ord-07478be766d54dbbb0b799c270f21f5c
Source dataset
uspto-grants-2015_08
Patent number
US09102591B2

Reaction notes

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