4-Bromopyridinium chloride → HCID 58159664, compound

HRID 240837Notes

Reaction equation

HRID 240837 reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:10]3[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=3)[CH:8]=2)[CH:3]=[CH:2]1.Cl.Br[C:19]1[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=1>>[N:22]1[CH:23]=[CH:24][C:19]([N:1]2[C:9]3[C:4](=[CH:5][CH:6]=[C:7]([C:10]4[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=4)[CH:8]=3)[CH:3]=[CH:2]2)=[CH:20][CH:21]=1

Participants

3

Reactant 2

HCID 881004-Bromopyridinium chlorideHCID 66955053HCID 66955053, compound

Product 1

HCID 58159664HCID 58159664, compound

Procedure

The target compound was prepared as in Example 1 using 4-(1H-indol-6-yl)phenol (200 mg, 0.96 mmol) and 4-bromopyridine hydrochloride (205 mg, 1.06 mmol).

Sources & evidence

ORD record
ord-cace42d13e06410aa597a142573722cf
Source dataset
uspto-grants-2014_02
Patent number
US08648089B2

Reaction notes

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