Ethyl benzoylacetate → HCID 178468498, compound

HRID 489368Notes

Reaction equation

HRID 489368 reaction equation
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH:5]=O.[NH2:11][C:12]1[CH:16]=[CH:15][NH:14][N:13]=1.[C:17]([CH2:25][C:26]([O:28][CH2:29][CH3:30])=[O:27])(=O)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[CH3:1][O:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH:5]1[C:25]([C:26]([O:28][CH2:29][CH3:30])=[O:27])=[C:17]([C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[NH:11][C:12]2=[N:13][NH:14][CH:15]=[C:16]12

Participants

4

Procedure

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

Sources & evidence

ORD record
ord-9b5b8572bf374b2ab8a3aebd1fdda958
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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