4-Chlorophenylboronic acid → HCID 21931051, compound

HRID 1243973Notes

Reaction equation

HRID 1243973 reaction equation
[CH3:1][O:2][C:3]1[CH:20]=[CH:19][C:6]([O:7][C:8]2[CH:13]=[CH:12][C:11]([C:14]3[CH:18]=[CH:17][NH:16][N:15]=3)=[CH:10][CH:9]=2)=[CH:5][CH:4]=1.[Cl:21][C:22]1[CH:27]=[CH:26][C:25](B(O)O)=[CH:24][CH:23]=1>>[Cl:21][C:22]1[CH:27]=[CH:26][C:25]([N:16]2[CH:17]=[CH:18][C:14]([C:11]3[CH:12]=[CH:13][C:8]([O:7][C:6]4[CH:19]=[CH:20][C:3]([O:2][CH3:1])=[CH:4][CH:5]=4)=[CH:9][CH:10]=3)=[N:15]2)=[CH:24][CH:23]=1

Participants

3

Reactant 2

HCID 742994-Chlorophenylboronic acidHCID 178492462HCID 178492462, compound

Product 1

HCID 21931051HCID 21931051, compound

Procedure

By the same procedure as Example 67 Part C, 3-[4-(4-methoxy-phenoxy)-phenyl]-1H-pyrazole and 4-chlorophenylboronic acid were converted to the title compound. MS m/z: ESI+ 377.1 (M+H)+.

Sources & evidence

ORD record
ord-a6c6f08098504a06b278907dc9bb871d
Source dataset
uspto-grants-2006_10
Patent number
US07119201B2

Reaction notes

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