4-Fluorophenylboronic acid → HCID 178505554, compound

HRID 2100970Notes

Reaction equation

HRID 2100970 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]=[CH:16][NH:15][N:14]=2)[N:3]=1.[F:18][C:19]1[CH:24]=[CH:23][C:22](B(O)O)=[CH:21][CH:20]=1>>[F:18][C:19]1[CH:24]=[CH:23][C:22]([C:2]2[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[CH:5]=[C:4]([NH:12][C:13]3[CH:17]=[CH:16][NH:15][N:14]=3)[N:3]=2)=[CH:21][CH:20]=1

Participants

3

Reactant 2

HCID 2856454-Fluorophenylboronic acidHCID 178478391HCID 178478391, compound

Product 1

HCID 178505554HCID 178505554, compound

Procedure

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

Sources & evidence

ORD record
ord-19437a72a634427e9787eb46716008ee
Source dataset
uspto-grants-2009_08
Patent number
US07572809B2

Reaction notes

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