(3-hydroxyphenyl)boronic Acid → HCID 66914362, compound

HRID 2104857Notes

Reaction equation

HRID 2104857 reaction equation
Br[C:2]1[C:11]2[C:6](=[C:7](Cl)[CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[OH:19][C:20]1[CH:21]=[C:22](B(O)O)[CH:23]=[CH:24][CH:25]=1>>[C:13]1([C:3]2[CH:4]=[N:5][C:6]3[C:11]([C:2]=2[C:24]2[CH:25]=[C:20]([OH:19])[CH:21]=[CH:22][CH:23]=2)=[CH:10][CH:9]=[CH:8][C:7]=3[C:24]2[CH:25]=[C:20]([OH:19])[CH:21]=[CH:22][CH:23]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Participants

3

Reactant 2

HCID 2734359(3-hydroxyphenyl)boronic AcidHCID 66914000HCID 66914000, compound

Product 1

HCID 66914362HCID 66914362, compound

Procedure

This compound was prepared according to the procedure of example 1, substituting 4-bromo-8-chloro-3-phenyl-quinoline and 3-hydroxybenzeneboronic acid MS (ESI) m/z 390.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-b7646ceccfe5408d80be9cb1d584c522
Source dataset
uspto-grants-2009_08
Patent number
US07576215B2

Reaction notes

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