Malononitrile, benzylidene- → 5-Aminomethyl-2-(1H-indol-2-yl)-6-phenyl-pyrimidin-4-ylamine

HRID 983872

Reaction equation

HRID 983872 reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[C:10]([NH2:12])=[NH:11].[CH:13](=[C:20]([C:23]#[N:24])[C:21]#[N:22])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[NH2:24][CH2:23][C:20]1[C:21]([NH2:22])=[N:11][C:10]([C:2]2[NH:1][C:9]3[C:4]([CH:3]=2)=[CH:5][CH:6]=[CH:7][CH:8]=3)=[N:12][C:13]=1[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Participants

3

Procedure

The title compound, MS: m/e=315.8 (M+H+), was prepared from 1H-indole-2-carboxamidine and 2-benzylidene-malononitrile in analogy to the process described in Example 11 as a solid.

Sources & evidence

ORD record
ord-cd638d4062e24c6680ebb0d3cc4cb564
Source dataset
uspto-grants-2005_03
Patent number
US06867205B2

Linked notes

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