(3-hydroxyphenyl)boronic Acid → HCID 66524287, compound

HRID 2104885Notes

Reaction equation

HRID 2104885 reaction equation
Br[C:2]1[C:11]2[C:6](=[C:7]([Cl:12])[CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[CH3:13].[OH:14][C:15]1[CH:16]=[C:17](B(O)O)[CH:18]=[CH:19][CH:20]=1>>[CH2:13]([C:3]1[CH:4]=[N:5][C:6]2[C:11]([C:2]=1[C:19]1[CH:20]=[C:15]([OH:14])[CH:16]=[CH:17][CH:18]=1)=[CH:10][CH:9]=[CH:8][C:7]=2[Cl:12])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1

Participants

3

Reactant 2

HCID 2734359(3-hydroxyphenyl)boronic AcidHCID 66914112HCID 66914112, compound

Product 1

HCID 66524287HCID 66524287, compound

Procedure

The title compound was prepared from 4-bromo-8-chloro-3-methyl-quinoline and 3-hydroxyphenyl boronic acid according to the procedure of Example 1. MS (ES) m/z 343.9.

Sources & evidence

ORD record
ord-440013f4f9d44c56867ac035a0c667a2
Source dataset
uspto-grants-2009_08
Patent number
US07576215B2

Reaction notes

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