4-Fluoro-N-(2,4,6,7-tetramethyl-3-phenyl-5-benzofuranyl)benzamide → HCID 10292741, compound
Reaction equation
[F:1][C:2]1[CH:29]=[CH:28][C:5]([C:6]([NH:8][C:9]2[C:10]([CH3:27])=[C:11]([CH3:26])[C:12]3[O:16][C:15]([CH3:17])=[C:14]([C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)[C:13]=3[C:24]=2[CH3:25])=O)=[CH:4][CH:3]=1>CO>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][NH:8][C:9]2[C:10]([CH3:27])=[C:11]([CH3:26])[C:12]3[O:16][C:15]([CH3:17])=[C:14]([C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=4)[C:13]=3[C:24]=2[CH3:25])=[CH:28][CH:29]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
By using 4-fluoro-N-(2,4,6,7-tetramethyl-3-phenyl-1-benzofuran-5-yl)benzamide, the title compound was synthesized according to Example 2b. Yield: 56%. Melting point: 135-136° C. (Methanol)
Sources & evidence
- ORD record
- ord-777b083ef43d4ae9851be876c4ee8eef
- Source dataset
- uspto-grants-2002_11
- Patent number
- US06479536B1
Reaction notes
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