1-Piperazinecarboxaldehyde → HCID 12817115, compound
Reaction equation
Cl[C:2]1[N:3]=[C:4]([N:21]2[CH2:26][CH2:25][S:24](=[O:27])[CH2:23][CH2:22]2)[C:5]2[N:11]=[CH:10][N:9]=[C:8]([NH:12][CH2:13][CH2:14][C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[C:6]=2[N:7]=1.[CH:28]([N:30]1[CH2:35][CH2:34][NH:33][CH2:32][CH2:31]1)=[O:29]>>[CH:28]([N:30]1[CH2:35][CH2:34][N:33]([C:2]2[N:3]=[C:4]([N:21]3[CH2:26][CH2:25][S:24](=[O:27])[CH2:23][CH2:22]3)[C:5]3[N:11]=[CH:10][N:9]=[C:8]([NH:12][CH2:13][CH2:14][C:15]4[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=4)[C:6]=3[N:7]=2)[CH2:32][CH2:31]1)=[O:29]Participants
3
Procedure
This compound was prepared analogous to Example 181 from 2-chloro-4-(1-oxido-thiomorpholino)-8-phenethylamino-pyrimido-[5,4-d]-pyrimidine (m.p.: 198°-200° C.) and N-formyl-piperazine.
Sources & evidence
- ORD record
- ord-7d56f2b5fa294c49869df8b0b7bcddf0
- Source dataset
- uspto-grants-1987_09
- Patent number
- US04690923
Reaction notes
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