5-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazine → HCID 22240231, compound

HRID 891913Notes

Reaction equation

HRID 891913 reaction equation
[CH:1]([C:4]1[CH:5]=[C:6](B2OC(C)(C)C(C)(C)O2)[CH:7]=[CH:8][CH:9]=1)([CH3:3])[CH3:2].[Cl:19][C:20]1[CH:21]=[C:22]([CH2:26][N:27]2[CH:31]=[CH:30][N:29]=[C:28]2[CH3:32])[N:23]=[N:24][CH:25]=1>>[ClH:19].[CH:1]([C:4]1[CH:9]=[C:8]([C:20]2[CH:21]=[C:22]([CH2:26][N:27]3[CH:31]=[CH:30][N:29]=[C:28]3[CH3:32])[N:23]=[N:24][CH:25]=2)[CH:7]=[CH:6][CH:5]=1)([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 117890255-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazineHCID 222401354,4,5,5-Tetramethyl-2-[3-(propan-2-yl)phenyl]-1,3,2-dioxaborolane

Product 1

HCID 22240231HCID 22240231, compound

Procedure

The title compound, MS: m/e=293.3 (M+H+), was prepared from 2-(3-isopropyl-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane and 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine.

Sources & evidence

ORD record
ord-60e7062341774d519f65cb111f4a21d5
Source dataset
uspto-grants-2006_02
Patent number
US07005432B2

Reaction notes

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