m-Chloroperbenzoic acid → HCID 118432144, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:12]([C:13]3[CH:14]=[C:15]([C:19]4[CH:24]=[CH:23][C:22]([S:25][CH3:26])=[CH:21][CH:20]=4)[CH:16]=[CH:17][CH:18]=3)[CH2:11][C:10]([C:27]([F:33])([F:32])[C:28]([F:31])([F:30])[F:29])=[N:9]2)=[CH:4][CH:3]=1.ClC1C=CC=C(C(OO)=[O:42])C=1>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:12]([C:13]3[CH:14]=[C:15]([C:19]4[CH:24]=[CH:23][C:22]([S:25]([CH3:26])=[O:42])=[CH:21][CH:20]=4)[CH:16]=[CH:17][CH:18]=3)[CH2:11][C:10]([C:27]([F:32])([F:33])[C:28]([F:29])([F:30])[F:31])=[N:9]2)=[CH:4][CH:3]=1Participants
3
Procedure
The compound of Example 40 was prepared in accordance with the same procedures as in Example 37, using the compound prepared in Example 23 and meta-chloroperbenzoic acid.
Sources & evidence
- ORD record
- ord-979ffa0d0ef14d298867ce4b6a1bbe9e
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09376420B2
Reaction notes
Loading…