5-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazine → HCID 22240308, compound

HRID 891933Notes

Reaction equation

HRID 891933 reaction equation
[F:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8](B(O)O)=[CH:9]2)=[CH:4][CH:3]=1.Cl[C:16]1[CH:17]=[C:18]([CH2:22][N:23]2[CH:27]=[CH:26][N:25]=[C:24]2[CH3:28])[N:19]=[N:20][CH:21]=1>>[F:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([C:16]3[CH:17]=[C:18]([CH2:22][N:23]4[CH:27]=[CH:26][N:25]=[C:24]4[CH3:28])[N:19]=[N:20][CH:21]=3)=[CH:9]2)=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 117890255-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazineHCID 22240184HCID 22240184, compound

Product 1

HCID 22240308HCID 22240308, compound

Procedure

The title compound, MS: m/e=319 (M+H+), was prepared from 7-fluoro-naphthalene-2-boronic acid and 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine.

Sources & evidence

ORD record
ord-34af337a5d654121a5e95d82ff6dc08d
Source dataset
uspto-grants-2006_02
Patent number
US07005432B2

Reaction notes

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