Piperazine → HCID 10049748, compound
Reaction equation
Cl[C:2]1[N:11]=[C:10]([N:12]2[CH2:17][CH2:16][S:15][CH2:14][CH2:13]2)[C:9]2[C:4](=[N:5][C:6]([NH:19][CH2:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[C:7]([Cl:18])[N:8]=2)[N:3]=1.[NH:27]1[CH2:32][CH2:31][NH:30][CH2:29][CH2:28]1>>[Cl:18][C:7]1[N:8]=[C:9]2[C:4](=[N:5][C:6]=1[NH:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[N:3]=[C:2]([N:27]1[CH2:32][CH2:31][NH:30][CH2:29][CH2:28]1)[N:11]=[C:10]2[N:12]1[CH2:17][CH2:16][S:15][CH2:14][CH2:13]1Participants
3
Procedure
This compound was prepared analogous to Example 1 from 2,6-dichloro-4-thiomorpholino-7-benzylamino-pteridine and piperazine.
Sources & evidence
- ORD record
- ord-8e4cf5b4c1c74626a5823c3c9d57d9f3
- Source dataset
- uspto-grants-1985_12
- Patent number
- US04560685
Reaction notes
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