Methyl Isocyanate → 5-Cyano-3-methyl-6-methylthio-1-phenyl-2,4(1H,3H)-pyrimidinedione
Reaction equation
[C:1]([C:3](=[C:9]([S:17][CH3:18])[NH:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[C:4]([O:6]CC)=O)#[N:2].[CH3:19][N:20]=[C:21]=[O:22]>>[C:1]([C:3]1[C:4](=[O:6])[N:20]([CH3:19])[C:21](=[O:22])[N:10]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:9]=1[S:17][CH3:18])#[N:2]Participants
3
Procedure
This compound was synthesized from ethyl 2-cyano-3-methylthio-3-phenylaminoacrylate and methyl isocyanate according to the same process as described in Example 92b. Yield=27%.
Sources & evidence
- ORD record
- ord-e2c1daaeb9d6451384ae9c2525971d3e
- Source dataset
- uspto-grants-1998_04
- Patent number
- US05736550
Reaction notes
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