Ethyl 3-oxohexanoate → HCID 178439495, compound

HRID 489339Notes

Reaction equation

HRID 489339 reaction equation
[CH2:1]([O:8][C:9]1[CH:16]=[CH:15][CH:14]=[CH:13][C:10]=1[CH:11]=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:17][C:18]1[CH:22]=[CH:21][NH:20][N:19]=1.O=[C:24]([CH2:31][CH2:32][CH3:33])[CH2:25][C:26]([O:28][CH2:29][CH3:30])=[O:27]>>[CH2:1]([O:8][C:9]1[CH:16]=[CH:15][CH:14]=[CH:13][C:10]=1[CH:11]1[C:25]([C:26]([O:28][CH2:29][CH3:30])=[O:27])=[C:24]([CH2:31][CH2:32][CH3:33])[NH:17][C:18]2=[N:19][NH:20][CH:21]=[C:22]12)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

4

Procedure

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

Sources & evidence

ORD record
ord-09252acc1c744babb4ba93650c0c14f1
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

Loading…