4-Bromopyridinium chloride → HCID 50991464, compound

HRID 240841Notes

Reaction equation

HRID 240841 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([C:10]2[CH:18]=[C:17]3[C:13]([CH:14]=[CH:15][N:16]3[C:19]3[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=3)=[CH:12][CH:11]=2)[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].Cl.[Br:26]C1C=CN=CC=1>>[Br:26][C:14]1[C:13]2[C:17](=[CH:18][C:10]([C:6]3[CH:7]=[CH:8][CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=3)=[CH:11][CH:12]=2)[N:16]([C:19]2[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=2)[CH:15]=1

Participants

3

Reactant 2

HCID 881004-Bromopyridinium chlorideHCID 58159639HCID 58159639, compound

Product 1

HCID 50991464HCID 50991464, compound

Procedure

The target compound was prepared as in Example 1 using 6-(3-nitrophenyl)-1-(pyridin-4-yl)-1H-indole (70 mg, 0.222 mmol) and 4-bromopyridine hydrochloride (40 mg, 0.222 mmol).

Sources & evidence

ORD record
ord-2bc019a1c0ae4547bd74e8c94d073dc9
Source dataset
uspto-grants-2014_02
Patent number
US08648089B2

Reaction notes

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