Veratroyl chloride → HCID 66882975, compound
Reaction equation
[CH:1]1([CH2:4][O:5][C:6]2[CH:7]=[C:8]([CH:12]=[CH:13][C:14]=2[O:15][CH:16]([F:18])[F:17])[C:9](Cl)=[O:10])[CH2:3][CH2:2]1.[Cl:19][C:20]1[CH:21]=[N:22][CH:23]=[C:24]([Cl:27])[C:25]=1[CH3:26].[CH3:28][O:29][C:30]1[CH:31]=[C:32]([CH:36]=[CH:37][C:38]=1[O:39][CH3:40])[C:33](Cl)=[O:34]>>[CH:1]1([CH2:4][O:5][C:6]2[CH:7]=[C:8](/[C:9](/[O:10][C:33](=[O:34])[C:32]3[CH:36]=[CH:37][C:38]([O:39][CH3:40])=[C:30]([O:29][CH3:28])[CH:31]=3)=[CH:26]/[C:25]3[C:24]([Cl:27])=[CH:23][N:22]=[CH:21][C:20]=3[Cl:19])[CH:12]=[CH:13][C:14]=2[O:15][CH:16]([F:18])[F:17])[CH2:3][CH2:2]1Participants
4
Procedure
The compound was obtained starting from 3-cyclopropylmethoxy-4-difluoromethoxy -benzoyl chloride, 3,5-dichloro-4-methylpyridine and 3,4-dimethoxy-benzoyl chloride, following the procedure of Example 24.
Workup
- customThe compound was obtained
Sources & evidence
- ORD record
- ord-7c493faa25ea4d61b1c2515871a54248
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07671066B2
Reaction notes
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