2,4-Dichlorobenzylidenemalononitrile → HCID 10288085, compound

HRID 983871Notes

Reaction equation

HRID 983871 reaction equation
[CH:1]1[C:9]2[C:8]3[CH:10]=[CH:11][CH:12]=[CH:13][C:7]=3[O:6][C:5]=2[CH:4]=[CH:3][C:2]=1[C:14]([NH2:16])=[NH:15].[Cl:17][C:18]1[CH:29]=[C:28]([Cl:30])[CH:27]=[CH:26][C:19]=1[CH:20]=[C:21]([C:24]#[N:25])[C:22]#[N:23]>>[NH2:25][CH2:24][C:21]1[C:22]([NH2:23])=[N:15][C:14]([C:2]2[CH:3]=[CH:4][C:5]3[O:6][C:7]4[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=4[C:9]=3[CH:1]=2)=[N:16][C:20]=1[C:19]1[CH:26]=[CH:27][C:28]([Cl:30])=[CH:29][C:18]=1[Cl:17]

Participants

3

Procedure

The title compound, MS: m/e=434.9 (M+), was prepared from dibenzofuran-2-carboxamidine and 2-(2,4-dichloro-benzylidene)-malononitrile in analogy to the process described in Example 11 as a solid.

Sources & evidence

ORD record
ord-0a1be1300f90420e9cd41ddd7104eabf
Source dataset
uspto-grants-2005_03
Patent number
US06867205B2

Reaction notes

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