Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[C:20](=[O:21])[N:19]([CH3:22])[C:12]2[N:13]=[C:14](SC)[N:15]=[CH:16][C:11]=2[CH:10]=1.[CH3:23][NH:24][CH3:25]>>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[C:20](=[O:21])[N:19]([CH3:22])[C:12]2[N:13]=[C:14]([N:24]([CH3:25])[CH3:23])[N:15]=[CH:16][C:11]=2[CH:10]=1Participants
3
Procedure
This compound was prepared by a procedure similar to that described in Example 40 starting with 6-(2,6-dichlorophenyl)-8-methyl-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 37 and dimethylamine gas; mp 256°-258° C.
Workup
- customThis compound was prepared by a procedure similar to
Sources & evidence
- ORD record
- ord-3649f27493174d968301ce7cf9e817e4
- Source dataset
- uspto-grants-1998_03
- Patent number
- US05733914
Linked notes
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