4-Methyl-3-thiopheneboronic acid → HCID 57799493, compound

HRID 2100935Notes

Reaction equation

HRID 2100935 reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:12][CH3:13])=[CH:9][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.[CH3:21][C:22]1[C:23](B(O)O)=[CH:24][S:25][CH:26]=1>>[CH3:20][C:18]1[NH:17][N:16]=[C:15]([NH:14][C:4]2[N:3]=[C:2]([C:23]3[C:22]([CH3:21])=[CH:26][S:25][CH:24]=3)[C:11]3[C:6]([CH:5]=2)=[CH:7][C:8]([O:12][CH3:13])=[CH:9][CH:10]=3)[CH:19]=1

Participants

3

Reactant 2

HCID 50839314-Methyl-3-thiopheneboronic acidHCID 57799674(1-chloro-6-methoxy-isoquinolin-3-yl)-(5-methyl-1H-pyrazol-3-yl)-amine

Product 1

HCID 57799493HCID 57799493, compound

Procedure

Similar procedure as described in example 131 was used, starting from (1-chloro-6-methoxy-isoquinolin-3-yl)-(5-methyl-1H-pyrazol-3-yl)-amine and 4-methyl-thiophene-3-boronic acid to give (5-methyl-1H-pyrazol-3-yl)-[1-(4-methyl-thiophen-3-yl)-6-methoxy-isoquinolin-3-yl]-amine. LC-MS m/e 351(MH+).

Sources & evidence

ORD record
ord-272c8c0730674aa4916e29fa4c1306cf
Source dataset
uspto-grants-2009_08
Patent number
US07572809B2

Reaction notes

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