4-Acetamidopiperidine → HCID 13043581, compound
Reaction equation
[CH2:1]([S:8][C:9]1[C:14]2[N:15]=[C:16](Cl)[N:17]=[C:18]([N:19]3[CH2:24][CH2:23][S:22](=[O:25])[CH2:21][CH2:20]3)[C:13]=2[N:12]=[CH:11][N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:27]([NH:30][CH:31]1[CH2:36][CH2:35][NH:34][CH2:33][CH2:32]1)(=[O:29])[CH3:28]>>[C:27]([NH:30][CH:31]1[CH2:36][CH2:35][N:34]([C:16]2[N:17]=[C:18]([N:19]3[CH2:24][CH2:23][S:22](=[O:25])[CH2:21][CH2:20]3)[C:13]3[N:12]=[CH:11][N:10]=[C:9]([S:8][CH2:1][C:2]4[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=4)[C:14]=3[N:15]=2)[CH2:33][CH2:32]1)(=[O:29])[CH3:28]Participants
3
Procedure
This compound was prepared analogous to Example 1 from 8-benzylthio-2-chloro-4-(1-oxido-thiomorpholino)pyrimido[5,4-d]pyrimidine and 4-acetylamino-piperidine.
Sources & evidence
- ORD record
- ord-f37fa4fdfa584e7fb716cf4301037a6e
- Source dataset
- uspto-grants-1984_10
- Patent number
- US04478833
Reaction notes
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