HCID 12576394, compound → HCID 15678765, compound

HRID 1090188Notes

Reaction equation

HRID 1090188 reaction equation
Cl.[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][N:10]([C:12]2[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=2)N)=[CH:5][CH:4]=1.O=[C:21]([CH2:29][CH3:30])[CH2:22][CH2:23][CH2:24][C:25]([O:27]C)=[O:26]>C(O)C>[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][N:10]2[C:12]3[C:17](=[CH:16][C:15]([O:18][CH3:19])=[CH:14][CH:13]=3)[C:29]([CH3:30])=[C:21]2[CH2:22][CH2:23][CH2:24][C:25]([OH:27])=[O:26])=[CH:5][CH:4]=1

Participants

4

Reactant 2

HCID 12576394HCID 12576394, compoundHCID 189475691-(4-Chlorobenzyl)-1-(4-methoxyphenyl)hydrazine hydrochloride

Product 1

HCID 15678765HCID 15678765, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Following the procedure of Example 2, but using 1-[(4-chlorophenyl)methyl]-1-(4-methoxyphenyl)hydrazine hydrochloride and methyl 5-oxoheptanoate as the starting materials and ethanol as the solvent, the title compound was prepared.

Sources & evidence

ORD record
ord-f6e8c40a15b0464f8bc627a05df88903
Source dataset
uspto-grants-1992_01
Patent number
US05081145

Reaction notes

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