Alpha-Methylstyrene → HCID 136348779, compound
Reaction equation
I[C:2]1[C:3]([O:24]C)=[CH:4][C:5]([O:22]C)=[C:6]([C:8]2[N:12]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[N+:19]([O-])=O)[N:11]=[CH:10][CH:9]=2)[CH:7]=1.[C:26]([C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)([CH3:28])=[CH2:27]>CCOCC>[C:29]1([CH:26]([CH3:28])[CH2:27][C:2]2[C:3]([OH:24])=[CH:4][C:5]([OH:22])=[C:6]([C:8]3[N:12]([C:13]4[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=4[NH2:19])[N:11]=[CH:10][CH:9]=3)[CH:7]=2)[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
12.8 Analogous reaction of 5-[5-iodo-2,4-dimethoxyphenyl]1-(2-nitrophenyl)-1H-pyrazole with isopropenylbenzene, hydrogenation and ether cleavage gives the compound 5-{5-(2-phenylpropyl)-2,4-dihydroxyphenyl}-1-(2-aminophenyl)-1H-pyrazole.
Sources & evidence
- ORD record
- ord-af8004997f5344838a92cff6c5b1df08
- Source dataset
- uspto-grants-2011_04
- Patent number
- US07932401B2
Reaction notes
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