2,6-Dimethylphenol → HCID 66922360, compound
Reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:14]([C:16]2[C:20]3=[N:21][CH:22]=[C:23]([O:25][CH2:26][CH3:27])[CH:24]=[C:19]3[N:18]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[C:17]=2Cl)=[O:15])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:35][C:36]1[CH:41]=[CH:40][CH:39]=[C:38]([CH3:42])[C:37]=1[OH:43]>>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:14]([C:16]2[C:20]3=[N:21][CH:22]=[C:23]([O:25][CH2:26][CH3:27])[CH:24]=[C:19]3[N:18]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[C:17]=2[O:43][C:37]2[C:38]([CH3:42])=[CH:39][CH:40]=[CH:41][C:36]=2[CH3:35])=[O:15])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]Participants
3
Procedure
The title compound was prepared from the compound of example 54, step 7, (290 mg, 598 μmol) and 2,6-dimethylphenol analogously as described in example 1, step 6.
Sources & evidence
- ORD record
- ord-0a802d70c0de421897bef2c0f0abe727
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08580813B2
Reaction notes
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