4-Bromopyridinium chloride → HCID 58159639, compound

HRID 2192249Notes

Reaction equation

HRID 2192249 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][NH:16]3)=[CH:12][CH:11]=2)[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].Cl.Br[C:21]1[CH:26]=[CH:25][N:24]=[CH:23][CH:22]=1>>[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:21]3[CH:26]=[CH:25][N:24]=[CH:23][CH:22]=3)=[CH:12][CH:11]=2)[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2]

Participants

3

Reactant 2

HCID 881004-Bromopyridinium chlorideHCID 66955149HCID 66955149, compound

Product 1

HCID 58159639HCID 58159639, compound

Procedure

The target compound was prepared as in Example 1 using 6-(3-nitrophenyl)-1H-indole (98 mg, 0.412 mmol) and 4-bromopyridine hydrochloride (88 mg, 0.453 mmol).

Sources & evidence

ORD record
ord-39ff9bf38287466fbec90315d893e3c8
Source dataset
uspto-grants-2012_12
Patent number
US08329708B2

Reaction notes

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