2,6-Dimethylphenol → HCID 66922229, compound

HRID 2039856Notes

Reaction equation

HRID 2039856 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[CH:21]=[N:22][C:23]([O:25][CH3:26])=[CH:24][C:19]=3[N:18]([CH:27]3[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]3)[C:17]=2Cl)=[O:15])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:34][C:35]1[CH:40]=[CH:39][CH:38]=[C:37]([CH3:41])[C:36]=1[OH:42]>>[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:14]([C:16]2[C:20]3[CH:21]=[N:22][C:23]([O:25][CH3:26])=[CH:24][C:19]=3[N:18]([CH:27]3[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]3)[C:17]=2[O:42][C:36]2[C:37]([CH3:41])=[CH:38][CH:39]=[CH:40][C:35]=2[CH3:34])=[O:15])[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 113352,6-DimethylphenolHCID 66922139HCID 66922139, compound

Product 1

HCID 66922229HCID 66922229, compound

Procedure

The title compound was prepared from the compound of example 46, step 7, (180 mg, 377 μmol) and 2,6-dimethylphenol analogously as described in example 1, step 6.

Sources & evidence

ORD record
ord-540856fd2a3a42b8bc648e003b86ea9e
Source dataset
uspto-grants-2013_11
Patent number
US08580813B2

Reaction notes

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