Methyl 2,2-dimethyl-4-oxohexanoate → 3-[1-(4-nitrobenzyl)-5-methoxy-3-methyl-1H-indol-2-yl]-2,2-dimethyl propanoic acid

HRID 1090206Notes

Reaction equation

HRID 1090206 reaction equation
Cl.[N+:2]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][N:12]([C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)N)=[CH:7][CH:6]=1)([O-:4])=[O:3].[CH3:22][C:23]([CH3:33])([CH2:28][C:29](=O)[CH2:30][CH3:31])[C:24]([O:26]C)=[O:25]>C(O)(C)(C)C>[N+:2]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][N:12]2[C:14]3[C:19](=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=3)[C:30]([CH3:31])=[C:29]2[CH2:28][C:23]([CH3:33])([CH3:22])[C:24]([OH:26])=[O:25])=[CH:7][CH:6]=1)([O-:4])=[O:3]

Participants

4

Reactant 2

HCID 13164740Methyl 2,2-dimethyl-4-oxohexanoateHCID 70472787(4-Nitrophenyl)methyl-1-(4-methoxyphenyl) hydrazine hydrochloride

Product 1

HCID 156788113-[1-(4-nitrobenzyl)-5-methoxy-3-methyl-1H-indol-2-yl]-2,2-dimethyl propanoic acid

Reagents, catalysts & solvents 1

HCID 6386tert-ButanolSolvent

Procedure

Following the method of Example 2, but using 1-[(4-nitrophenyl)methyl-1-(4-methoxyphenyl) hydrazine hydrochloride and methyl 2,2-dimethyl-4-oxo-hexanoate as the starting materials and tert-butanol as the solvent, the title compound was prepared.

Sources & evidence

ORD record
ord-194aa907561a488a9bcb9b67b8c72082
Source dataset
uspto-grants-1992_01
Patent number
US05081145

Reaction notes

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