HCID 10135914, compound → HCID 9821830, compound

HRID 272404Notes

Reaction equation

HRID 272404 reaction equation
[F:1][C:2]1[CH:30]=[CH:29][C:5]([C:6]([NH:8][C:9]2[C:10]([CH3:28])=[C:11]([CH3:27])[C:12]3[O:16][C:15]([CH3:17])=[C:14]([C:18]4[CH:23]=[CH:22][C:21]([F:24])=[CH:20][CH:19]=4)[C:13]=3[C:25]=2[CH3:26])=O)=[CH:4][CH:3]=1>C(O)C>[F:1][C:2]1[CH:30]=[CH:29][C:5]([CH2:6][NH:8][C:9]2[C:10]([CH3:28])=[C:11]([CH3:27])[C:12]3[O:16][C:15]([CH3:17])=[C:14]([C:18]4[CH:23]=[CH:22][C:21]([F:24])=[CH:20][CH:19]=4)[C:13]=3[C:25]=2[CH3:26])=[CH:4][CH:3]=1

Participants

3

Reactant 1

HCID 10135914HCID 10135914, compound

Product 1

HCID 9821830HCID 9821830, compoundYield 66%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

By using 4-fluoro-N-[3-(4-fluorophenyl)-2,4,6,7-tetramethyl-1-benzofuran-5-yl]benzamide, the title compound was synthesized according to Example 2b. Yield: 66%. Melting point: 107-109° C. (Ethanol).

Sources & evidence

ORD record
ord-a14ee183ba4042b4951a56c44f76e691
Source dataset
uspto-grants-2008_11
Patent number
US07456162B2

Reaction notes

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