Thiomorpholine 1-oxide → 8-Benzylthio-2,4-bis-(1-oxido-thiomorpholino)-pyrimido[5,4-d]pyrimidine
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.[NH:27]1[CH2:32][CH2:31][S:30](=[O:33])[CH2:29][CH2:28]1>O1CCOCC1>[CH2:1]([S:8][C:9]1[C:14]2[N:15]=[C:16]([N:27]3[CH2:32][CH2:31][S:30](=[O:33])[CH2:29][CH2:28]3)[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]=1Participants
4
Procedure
This compound was prepared analogous to Example 1 from 8-benzylthio-2-chloro-4-(1-oxido-thiomorpholino)pyrimido[5,4-d]pyrimidine (melting point: 188°-190° C.) and thiomorpholine-1-oxide by refluxing for three hours in dioxane.
Sources & evidence
- ORD record
- ord-152e9c184bd3429c9385b6357b7776d8
- Source dataset
- uspto-grants-1984_10
- Patent number
- US04478833
Reaction notes
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