2-Methoxybenzaldehyde → HCID 178468901, compound

HRID 489426Notes

Reaction equation

HRID 489426 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]([CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])(=O)[CH:18]([CH3:20])[CH3:19]>>[CH3:1][O:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH:5]1[C:22]([C:23]([O:25][CH2:26][CH3:27])=[O:24])=[C:17]([CH:18]([CH3:20])[CH3:19])[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 isobutyrylacetate in the same manner as in Example 275.

Sources & evidence

ORD record
ord-4dfaff8436484150920b7aca10939c81
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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