2-Methoxybenzaldehyde → HCID 178494562, compound

HRID 489367Notes

Reaction equation

HRID 489367 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.[CH3:17][O:18][CH2:19][C:20](=O)[CH2:21][C:22]([O:24][CH3:25])=[O:23]>>[CH3:17][O:18][CH2:19][C:20]1[NH:11][C:12]2=[N:13][NH:14][CH:15]=[C:16]2[CH:5]([C:4]2[CH:7]=[CH:8][CH:9]=[CH:10][C:3]=2[O:2][CH3:1])[C:21]=1[C:22]([O:24][CH3:25])=[O:23]

Participants

4

Reactant 3

HCID 86582-MethoxybenzaldehydeHCID 123500Methyl 4-methoxyacetoacetateHCID 178418806HCID 178418806, compound

Product 1

HCID 178494562HCID 178494562, compound

Procedure

The title compound was prepared from 2-methoxybenzaldehyde, 3-aminopyrazole and methyl 4-methoxyacetoacetate in the same manner as in Example 1.

Sources & evidence

ORD record
ord-5f485f6b485a4d7aa4e75f39dca1571a
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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