Ethyl 3-oxohexanoate → HCID 178439515, compound

HRID 489349Notes

Reaction equation

HRID 489349 reaction equation
[Cl:1][C:2]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[CH:6][C:3]=1[CH:4]=O.[NH2:12][C:13]1[CH:17]=[CH:16][NH:15][N:14]=1.O=[C:19]([CH2:26][CH2:27][CH3:28])[CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22]>>[Cl:1][C:2]1[CH:9]=[CH:8][C:7]([O:10][CH3:11])=[CH:6][C:3]=1[CH:4]1[C:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[C:19]([CH2:26][CH2:27][CH3:28])[NH:12][C:13]2=[N:14][NH:15][CH:16]=[C:17]12

Participants

4

Reactant 3

HCID 238498Ethyl 3-oxohexanoateHCID 129278382-Chloro-5-methoxybenzaldehydeHCID 178418806HCID 178418806, compound

Product 1

HCID 178439515HCID 178439515, compound

Procedure

The title compound was prepared from 2-chloro-5-methoxybenzaldehyde, 3-aminopyrazole and ethyl 3-ketohexanoate in the same manner as in Example 25.

Sources & evidence

ORD record
ord-4a92c5f13f3b453887daa0e4c511b88b
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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