m-Chloroperbenzoic acid → HCID 118431636, compound

HRID 2207968Notes

Reaction equation

HRID 2207968 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[N:9]1[CH:13]([C:14]2[CH:15]=[C:16]([C:20]3[CH:25]=[CH:24][C:23]([S:26][CH3:27])=[CH:22][CH:21]=3)[CH:17]=[CH:18][CH:19]=2)[CH2:12][C:11]([C:28]([F:34])([F:33])[C:29]([F:32])([F:31])[F:30])=[N:10]1.ClC1C=CC=C(C(OO)=[O:43])C=1>>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[N:9]1[CH:13]([C:14]2[CH:15]=[C:16]([C:20]3[CH:25]=[CH:24][C:23]([S:26]([CH3:27])=[O:43])=[CH:22][CH:21]=3)[CH:17]=[CH:18][CH:19]=2)[CH2:12][C:11]([C:28]([F:33])([F:34])[C:29]([F:32])([F:30])[F:31])=[N:10]1

Participants

3

Reactant 2

HCID 70297m-Chloroperbenzoic acidHCID 118432140HCID 118432140, compound

Product 1

HCID 118431636HCID 118431636, compound

Procedure

The compound of Example 42 was prepared in accordance with the same procedures as in Example 37, using the compound prepared in Example 25 and meta-chloroperbenzoic acid.

Sources & evidence

ORD record
ord-c9ae2595804c4114b77275dc955c7d76
Source dataset
uspto-grants-2016_06
Patent number
US09376420B2

Reaction notes

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