m-Chloroperbenzoic acid → HCID 23365366, compound

HRID 1493233Notes

Reaction equation

HRID 1493233 reaction equation
[Cl:1][C:2]1[CH:25]=[CH:24][C:5]([CH2:6][O:7][C:8]2[CH:9]=[N:10][CH:11]=[CH:12][C:13]=2[CH:14]([N:19]2[CH:23]=[CH:22][N:21]=[CH:20]2)[CH2:15][CH2:16][CH2:17][CH3:18])=[CH:4][CH:3]=1.ClC1C=CC=C(C(OO)=[O:34])C=1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][O:7][C:8]2[CH:9]=[N+:10]([O-:34])[CH:11]=[CH:12][C:13]=2[CH:14]([N:19]2[CH:23]=[CH:22][N:21]=[CH:20]2)[CH2:15][CH2:16][CH2:17][CH3:18])=[CH:24][CH:25]=1

Participants

3

Reactant 2

HCID 70297m-Chloroperbenzoic acidHCID 23365339HCID 23365339, compound

Product 1

HCID 23365366HCID 23365366, compound

Procedure

0.624 g of 3-(4-chlorobenzyloxy)-4-[1-(1-imidazolyl)-pentyl]-pyridine is reacted analogously to example 15 with 0.410 g of m-chloroperbenzoic acid to the title compound.

Sources & evidence

ORD record
ord-bd943140a373452294b3f4d0b3c4edc8
Source dataset
uspto-grants-1991_06
Patent number
US05021434

Reaction notes

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