2,4-Dichlorobenzylidenemalononitrile → HCID 10237546, compound

HRID 983870Notes

Reaction equation

HRID 983870 reaction equation
[F:1][C:2]1[CH:12]=[CH:11][C:5]([O:6][CH2:7][C:8]([NH2:10])=[NH:9])=[CH:4][CH:3]=1.[Cl:13][C:14]1[CH:25]=[C:24]([Cl:26])[CH:23]=[CH:22][C:15]=1[CH:16]=[C:17]([C:20]#[N:21])[C:18]#[N:19]>>[NH2:21][CH2:20][C:17]1[C:18]([NH2:19])=[N:9][C:8]([CH2:7][O:6][C:5]2[CH:4]=[CH:3][C:2]([F:1])=[CH:12][CH:11]=2)=[N:10][C:16]=1[C:15]1[CH:22]=[CH:23][C:24]([Cl:26])=[CH:25][C:14]=1[Cl:13]

Participants

3

Reactant 2

HCID 180892,4-DichlorobenzylidenemalononitrileHCID 27746842-(4-FLUORO-PHENOXY)-ACETAMIDINE

Product 1

HCID 10237546HCID 10237546, compound

Procedure

The title compound, MS: m/e=392.8 (M+H+), was prepared from 2-(4-fluoro-phenoxy)-acetamidine and 2-(2,4-dichloro-benzylidene)-malononitrile in analogy to the process described in Example 11 as a solid.

Sources & evidence

ORD record
ord-8e357a355ce64f019aa0abc27fdf9713
Source dataset
uspto-grants-2005_03
Patent number
US06867205B2

Reaction notes

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