2-Chlorobenzaldehyde → HCID 178429603, compound

HRID 489310Notes

Reaction equation

HRID 489310 reaction equation
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=O.[NH2:10][C:11]1[CH:15]=[CH:14][NH:13][N:12]=1.[C:16]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])(=[O:21])[CH2:17][C:18]([CH3:20])=O>>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]1[C:17]([C:16]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])=[C:18]([CH3:20])[NH:10][C:11]2=[N:12][NH:13][CH:14]=[C:15]12

Participants

4

Reactant 3

HCID 69962-ChlorobenzaldehydeHCID 15538Tert-butyl acetoacetateHCID 178418806HCID 178418806, compound

Product 1

HCID 178429603HCID 178429603, compound

Procedure

The title compound was prepared from 2-chlorobenzaldehyde, 3-aminopyrazole and t-butyl acetoacetate in the same manner as in Example 1.

Sources & evidence

ORD record
ord-e76b2084f3a24554ada70fca1faf0383
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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