1-Methyl-1H-pyrazole-4-boronic acid → HCID 68858768, compound

HRID 2100950Notes

Reaction equation

HRID 2100950 reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[CH:10]=2)[CH:5]=[C:4]([NH:14][C:15]2[CH:19]=[C:18]([CH3:20])[NH:17][N:16]=2)[N:3]=1.C[N:22]1[CH:26]=[C:25](B(O)O)[CH:24]=[N:23]1>>[CH3:20][C:18]1[NH:17][N:16]=[C:15]([NH:14][C:4]2[N:3]=[C:2]([C:25]3[CH:26]=[N:22][NH:23][CH:24]=3)[C:11]3[C:6]([CH:5]=2)=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[CH:10]=3)[CH:19]=1

Participants

3

Reactant 2

HCID 112635011-Methyl-1H-pyrazole-4-boronic acidHCID 57799818HCID 57799818, compound

Product 1

HCID 68858768HCID 68858768, compound

Procedure

Similar procedure as described in example 131 was used, starting from (1-chloro-7-methoxy-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)-7-methoxy-isoquinolin-3-yl]-amine. LC-MS m/e 335(MH+).

Sources & evidence

ORD record
ord-8e2a38faedb24363b137b9b373c42794
Source dataset
uspto-grants-2009_08
Patent number
US07572809B2

Reaction notes

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