Ethyl 3-oxohexanoate → HCID 178439501, compound

HRID 489344Notes

Reaction equation

HRID 489344 reaction equation
[Cl:1][C:2]1[C:9]([C:10]([F:13])([F:12])[F:11])=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=O.[NH2:14][C:15]1[CH:19]=[CH:18][NH:17][N:16]=1.O=[C:21]([CH2:28][CH2:29][CH3:30])[CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24]>>[Cl:1][C:2]1[C:9]([C:10]([F:13])([F:12])[F:11])=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]1[C:22]([C:23]([O:25][CH2:26][CH3:27])=[O:24])=[C:21]([CH2:28][CH2:29][CH3:30])[NH:14][C:15]2=[N:16][NH:17][CH:18]=[C:19]12

Participants

4

Reactant 3

HCID 238498Ethyl 3-oxohexanoateHCID 27366722-Chloro-3-(trifluoromethyl)benzaldehydeHCID 178418806HCID 178418806, compound

Product 1

HCID 178439501HCID 178439501, compound

Procedure

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

Sources & evidence

ORD record
ord-a14a59a409f1495eb83041ba99976a3b
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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