2,4-Dichlorobenzylidenemalononitrile → HCID 10238883, compound

HRID 983869Notes

Reaction equation

HRID 983869 reaction equation
[F:1][C:2]([F:17])([F:16])[C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([C:12]([F:15])([F:14])[F:13])[CH:11]=1)[C:6]([NH2:8])=[NH:7].[Cl:18][C:19]1[CH:30]=[C:29]([Cl:31])[CH:28]=[CH:27][C:20]=1[CH:21]=[C:22]([C:25]#[N:26])[C:23]#[N:24]>>[NH2:26][CH2:25][C:22]1[C:23]([NH2:24])=[N:7][C:6]([C:5]2[CH:4]=[C:3]([C:2]([F:16])([F:17])[F:1])[CH:11]=[C:10]([C:12]([F:15])([F:13])[F:14])[CH:9]=2)=[N:8][C:21]=1[C:20]1[CH:27]=[CH:28][C:29]([Cl:31])=[CH:30][C:19]=1[Cl:18]

Participants

3

Reactant 2

HCID 180892,4-DichlorobenzylidenemalononitrileHCID 2736102HCID 2736102, compound

Product 1

HCID 10238883HCID 10238883, compound

Procedure

The title compound, MS: m/e=481.2 (M+H+), was prepared from 3,5-bis-trifluoromethyl-benzamidine and 2-(2,4-dichloro-benzylidene)-malononitrile in analogy to the process described in Example 11 as a solid.

Sources & evidence

ORD record
ord-83595dfde4634cd0aab780c5a7630588
Source dataset
uspto-grants-2005_03
Patent number
US06867205B2

Reaction notes

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