5-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazine → HCID 22240153, compound

HRID 891927Notes

Reaction equation

HRID 891927 reaction equation
[CH3:1][O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][C:4]=1B1OC(C)(C)C(C)(C)O1.Cl[C:23]1[CH:24]=[C:25]([CH2:29][N:30]2[CH:34]=[CH:33][N:32]=[C:31]2[CH3:35])[N:26]=[N:27][CH:28]=1>>[CH3:1][O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=[CH:5][C:4]=1[C:23]1[CH:24]=[C:25]([CH2:29][N:30]2[CH:34]=[CH:33][N:32]=[C:31]2[CH3:35])[N:26]=[N:27][CH:28]=1

Participants

3

Reactant 2

HCID 117890255-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazineHCID 22240123HCID 22240123, compound

Product 1

HCID 22240153HCID 22240153, compound

Procedure

The title compound, MS: m/e=331.4 (M+H+), was prepared from 2-(1-methoxy-naphthalen-2-yl)-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-3b84ef8b658141efb0128b7f99401671
Source dataset
uspto-grants-2006_02
Patent number
US07005432B2

Reaction notes

Loading…