HCID 21961363, compound → HCID 15516565, compound

HRID 272334Notes

Reaction equation

HRID 272334 reaction equation
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[C:14]3[C:15]([CH3:32])=[C:16]([N:21]4[C:29](=O)[C:28]5[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=5)[C:22]4=O)[C:17]([CH3:20])=[C:18]([CH3:19])[C:13]=3[O:12][C:11]=2[CH3:33])=[CH:6][CH:5]=1)([CH3:3])[CH3:2]>C(O)C>[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[C:14]3[C:15]([CH3:32])=[C:16]([N:21]4[CH2:22][C:23]5[C:28](=[CH:27][CH:26]=[CH:25][CH:24]=5)[CH2:29]4)[C:17]([CH3:20])=[C:18]([CH3:19])[C:13]=3[O:12][C:11]=2[CH3:33])=[CH:6][CH:5]=1)([CH3:3])[CH3:2]

Participants

3

Reactant 1

HCID 21961363HCID 21961363, compound

Product 1

HCID 15516565HCID 15516565, compoundYield 70%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

By using 2-[3-(4-isopropylphenyl)-2,4,6,7-tetramethyl-1-benzofuran-5-yl]-1H-isoindole-1,3(2H)-dione, the title compound was synthesized according to Example 2a. Yield: 70%. Melting point: 126-129° C. (Ethanol)

Sources & evidence

ORD record
ord-163c2177ebd0433c8bdd1c3c914a6052
Source dataset
uspto-grants-2008_11
Patent number
US07456162B2

Reaction notes

Loading…