Dimethylamine → 2,4-Diamino-5-(2,4-dichlorophenyl)-6-dimethylaminomethylpyrimidine
Reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([C:9]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][C:10]=2[Cl:16])=[C:4]([CH2:17]Br)[N:3]=1.[CH3:19][NH:20][CH3:21]>C(O)C>[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([C:9]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][C:10]=2[Cl:16])=[C:4]([CH2:17][N:20]([CH3:21])[CH3:19])[N:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
This compound was prepared from 2,4-diamino-5-(2,4-dichlorophenyl)-6-bromomethyl-pyrimidine (Example 53) by reaction with dimethylamine in ethanol at room temperature, mp. 170°-172° C.
Sources & evidence
- ORD record
- ord-4f6a6faf1f7649a0b5d9b90e4b38082e
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05684005
Reaction notes
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