Reaction equation
[Cl:1][C:2]1[N:7]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[N:5]=[C:4]([O:14][CH2:15][CH2:16][CH:17]([CH3:19])[CH3:18])[CH:3]=1.ClC1C=C(Cl)N=[C:23]([C:28]2C=CC=[CH:30][CH:29]=2)N=1.ClC1C=C(Cl)N=C(CCCCCCCCCC)N=1>>[Cl:1][C:2]1[N:7]=[C:6]([CH2:8][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:23][CH2:28][CH2:29][CH3:30])[N:5]=[C:4]([O:14][CH2:15][CH2:16][CH:17]([CH3:18])[CH3:19])[CH:3]=1Participants
4
Procedure
The compound of Example 24 is prepared analogously to the compound of Example 3, with 4,6-dichloro-2-phenylpyrimidine being replaced by 4,6-dichloro-2-decylpyrimidine.
Sources & evidence
- ORD record
- ord-39d806576da54113922b16881543ca10
- Source dataset
- uspto-grants-1994_08
- Patent number
- US05340701
Linked notes
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