HCID 10112309, compound → HCID 10222473, compound

HRID 272396Notes

Reaction equation

HRID 272396 reaction equation
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[C:14]3[C:15]([CH3:30])=[C:16]([NH:21][C:22](=O)[C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)[C:17]([CH3:20])=[C:18]([CH3:19])[C:13]=3[O:12][C:11]=2[CH3:31])=[CH:6][CH:5]=1)([CH3:3])[CH3:2]>C(O)C>[CH2:22]([NH:21][C:16]1[C:17]([CH3:20])=[C:18]([CH3:19])[C:13]2[O:12][C:11]([CH3:31])=[C:10]([C:7]3[CH:6]=[CH:5][C:4]([CH:1]([CH3:2])[CH3:3])=[CH:9][CH:8]=3)[C:14]=2[C:15]=1[CH3:30])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1

Participants

3

Reactant 1

HCID 10112309HCID 10112309, compound

Product 1

HCID 10222473HCID 10222473, compoundYield 55%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

By using N-[3-(4-isopropylphenyl)-2,4,6,7-tetramethyl-1-benzofuran-5-yl]benzamide, the title compound was synthesized according to Example 2b. Yield: 55%. Melting point: 94-95° C. (Ethanol).

Sources & evidence

ORD record
ord-af6f6bc5f64646769789f9b8a51a5718
Source dataset
uspto-grants-2008_11
Patent number
US07456162B2

Reaction notes

Loading…