Ethyl 3-oxohexanoate → HCID 135583922, compound
Reaction equation
[CH2:1]([C:5]1[CH:12]=[CH:11][CH:10]=[CH:9][C:6]=1[CH:7]=O)[CH2:2][CH2:3][CH3:4].[NH2:13][C:14]1[CH:18]=[CH:17][NH:16][N:15]=1.O=[C:20]([CH2:27][CH2:28][CH3:29])[CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23]>>[CH2:1]([C:5]1[CH:12]=[CH:11][CH:10]=[CH:9][C:6]=1[CH:7]1[C:21]([C:22]([O:24][CH2:25][CH3:26])=[O:23])=[C:20]([CH2:27][CH2:28][CH3:29])[NH:13][C:14]2[NH:15][N:16]=[CH:17][C:18]1=2)[CH2:2][CH2:3][CH3:4]Participants
4
Procedure
The title compound was prepared from 2-butylbenzaldehyde, 3-aminopyrazole and ethyl 3-ketohexanoate in the same manner as in Example 25.
Sources & evidence
- ORD record
- ord-cf5cffd9c9ea4d5f862b7f59ea46a9af
- Source dataset
- uspto-grants-2005_12
- Patent number
- US06977262B2
Reaction notes
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