Phenylboronic Acid → HCID 22001172, compound

HRID 324939Notes

Reaction equation

HRID 324939 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6](Br)=[C:5]([O:10][CH3:11])[C:4]=1[C:12]1[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=1.[C:18]1(B(O)O)[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[C:5]([O:10][CH3:11])[C:4]=1[C:12]1[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=1

Participants

3

Reactant 2

HCID 66827Phenylboronic AcidHCID 22001176HCID 22001176, compound

Product 1

HCID 22001172HCID 22001172, compound

Procedure

This compound was prepared by the same procedure as used in EXAMPLE 3 using 1,3-dimethoxy-2-(pyrid-3-yl)-4-bromobenzene 30 and phenyl boronic acid to yield 31.

Workup

  1. customThis compound was prepared by the same procedure

Sources & evidence

ORD record
ord-df6a1078747747728326ada30f043ac0
Source dataset
uspto-grants-2001_04
Patent number
US06221604B1

Reaction notes

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