5-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazine → HCID 22240219, compound

HRID 891915Notes

Reaction equation

HRID 891915 reaction equation
[CH3:1][O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6](B2OC(C)(C)C(C)(C)O2)=[CH:5][CH:4]=1.[Cl:22][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>>[ClH:22].[CH3:1][O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([C:23]2[CH:24]=[C:25]([CH2:29][N:30]3[CH:34]=[CH:33][N:32]=[C:31]3[CH3:35])[N:26]=[N:27][CH:28]=2)=[CH:5][CH:4]=1

Participants

3

Reactant 2

HCID 117890255-Chloro-3-(2-methylimidazol-1-ylmethyl)-pyridazineHCID 21923954HCID 21923954, compound

Product 1

HCID 22240219HCID 22240219, compound

Procedure

The title compound, MS: m/e=331.3 (M+H+), was prepared from 2-(4-methoxy-naphthalen-1-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-6552057ecd274deabf922bf2cf19491f
Source dataset
uspto-grants-2006_02
Patent number
US07005432B2

Reaction notes

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