2,6-Dichlorobenzaldehyde → HCID 178479171, compound

HRID 489460Notes

Reaction equation

HRID 489460 reaction equation
[NH:1]1[CH2:11][CH2:10][CH2:9][CH:3](C(OCC)=O)[CH2:2]1.[Cl:12][C:13]1[CH:20]=[CH:19][CH:18]=[C:17]([Cl:21])[C:14]=1[CH:15]=O.[NH2:22][C:23]1[CH:27]=[CH:26][NH:25][N:24]=1>>[ClH:12].[C:2]([C:3]1[CH:15]([C:14]2[C:13]([Cl:12])=[CH:20][CH:19]=[CH:18][C:17]=2[Cl:21])[C:27]2[C:23](=[N:24][NH:25][CH:26]=2)[NH:22][C:9]=1[CH:9]1[CH2:3][CH2:2][NH:1][CH2:11][CH2:10]1)#[N:1]

Participants

4

Reactant 3

HCID 67372,6-DichlorobenzaldehydeHCID 98969Ethyl nipecotateHCID 178418806HCID 178418806, compound

Product 1

HCID 178479171HCID 178479171, compound

Procedure

The title compound was prepared from ethyl nipecotate, 2,6-dichlorobenzaldehyde and 3-aminopyrazole in the same manner as in Examples 1001 and 1002.

Sources & evidence

ORD record
ord-d096774dcdac413c9fd96c5c872a32d0
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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