3,5-Dichlorophenylboronic acid → HCID 22240264, compound

HRID 891893Notes

Reaction equation

HRID 891893 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4](B(O)O)[CH:5]=[C:6]([Cl:8])[CH:7]=1.Cl[C:13]1[CH:14]=[C:15]([CH2:19][N:20]2[CH:24]=[CH:23][N:22]=[C:21]2[CH3:25])[N:16]=[N:17][CH:18]=1>>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([C:13]2[CH:14]=[C:15]([CH2:19][N:20]3[CH:24]=[CH:23][N:22]=[C:21]3[CH3:25])[N:16]=[N:17][CH:18]=2)[CH:5]=[C:6]([Cl:8])[CH:7]=1

Participants

3

Reactant 2

HCID 27343313,5-Dichlorophenylboronic acidHCID 117890255-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazine

Product 1

HCID 22240264HCID 22240264, compound

Procedure

The title compound, MS: m/e=319.3 (M+H+), was prepared from 3,5-dichlorobenzeneboronic acid and 5-chloro-3-(2-methyl-imidazol-1-ylmethyl)-pyridazine.

Sources & evidence

ORD record
ord-d7b06337aca74f3895a091079419ffce
Source dataset
uspto-grants-2006_02
Patent number
US07005432B2

Reaction notes

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