Ethyl 3-oxohexanoate → HCID 178439502, compound

HRID 489379Notes

Reaction equation

HRID 489379 reaction equation
[Cl:1][C:2]1[C:3]([CH3:10])=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=O.[NH2:11][C:12]1[CH:16]=[CH:15][NH:14][N:13]=1.O=[C:18]([CH2:25][CH2:26][CH3:27])[CH2:19][C:20]([O:22][CH2:23][CH3:24])=[O:21]>>[Cl:1][C:2]1[C:3]([CH3:10])=[C:4]([CH:5]2[C:19]([C:20]([O:22][CH2:23][CH3:24])=[O:21])=[C:18]([CH2:25][CH2:26][CH3:27])[NH:11][C:12]3=[N:13][NH:14][CH:15]=[C:16]23)[CH:7]=[CH:8][CH:9]=1

Participants

4

Reactant 3

HCID 238498Ethyl 3-oxohexanoateHCID 131626623-Chloro-2-methylbenzaldehydeHCID 178418806HCID 178418806, compound

Product 1

HCID 178439502HCID 178439502, compound

Procedure

The title compound was prepared from 3-chloro-2-methylbenzaldehyde, 3-aminopyrazole and ethyl 3-ketohexanoate in the same manner as in Example 1.

Sources & evidence

ORD record
ord-7e5be02ba693450abdf718ce8903ba57
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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