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2-Chlorobenzaldehyde → HCID 178439479, compound

HRID 489329
Notes
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Reaction equation

HRID 489329 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.O=[C:17]([CH2:23][CH2:24][CH3:25])[CH2:18][C:19]([O:21][CH3:22])=[O:20]>>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]1[C:18]([C:19]([O:21][CH3:22])=[O:20])=[C:17]([CH2:23][CH2:24][CH3:25])[NH:10][C:11]2=[N:12][NH:13][CH:14]=[C:15]12
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 69962-ChlorobenzaldehydeHCID 121700Methyl 3-oxohexanoateHCID 178418806HCID 178418806, compound

Product 1

HCID 178439479HCID 178439479, compound

Procedure

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

Sources & evidence

ORD record
ord-83ede6e26ae2422f98588275659f2321
Source dataset
uspto-grants-2005_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06977262B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes