1-Methyl-1H-pyrazole-4-boronic acid → HCID 57799752, compound

HRID 2100911Notes

Reaction equation

HRID 2100911 reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4]([NH:12][C:13]2[CH:17]=[C:16]([CH3:18])[NH:15][N:14]=2)[N:3]=1.C[N:20]1[CH:24]=[C:23](B(O)O)[CH:22]=[N:21]1>>[CH3:18][C:16]1[NH:15][N:14]=[C:13]([NH:12][C:4]2[N:3]=[C:2]([C:23]3[CH:24]=[N:20][NH:21][CH:22]=3)[C:11]3[C:6]([CH:5]=2)=[CH:7][CH:8]=[CH:9][CH:10]=3)[CH:17]=1

Participants

3

Reactant 2

HCID 112635011-Methyl-1H-pyrazole-4-boronic acidHCID 57799635(1-chloro-isoquinolin-3-yl)-(5-methyl-1H-pyrazol-3-yl)-amine

Product 1

HCID 57799752HCID 57799752, compound

Procedure

Similar procedure as described in example 131 was used, starting from (1-chloro-isoquinolin-3-yl)-(5-methyl-1H-pyrazol-3-yl)-amine and N-methyl-pyrazole-4-boronic acid to give (5-methyl-1H-pyrazol-3-yl)-[1-(1H-pyrazol-4-yl)-isoquinolin-3-yl]-amine. LC-MS m/e 305(MH+).

Sources & evidence

ORD record
ord-48e778259b474b4a8c26dc5899c887ef
Source dataset
uspto-grants-2009_08
Patent number
US07572809B2

Reaction notes

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