1-Methylpiperazine → 1,2,4-Triazine, 5,6-bis(4-methoxyphenyl)-3-(4-methyl-1-piperazinyl)-
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[N:10]=[C:11](SC)[N:12]=[N:13][C:14]=2[C:15]2[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=2)=[CH:5][CH:4]=1.[CH3:25][N:26]1[CH2:31][CH2:30][NH:29][CH2:28][CH2:27]1>O>[CH3:25][N:26]1[CH2:31][CH2:30][N:29]([C:11]2[N:12]=[N:13][C:14]([C:15]3[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=3)=[C:9]([C:6]3[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=3)[N:10]=2)[CH2:28][CH2:27]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Ten grams of 5,6-bis(4-methoxyphenyl)-3-methylthio-1,2,4-triazine and 40 ml. of N-methylpiperazine were refluxed for 12 hours. The reaction mixture was poured into water and the solid product was collected. The product was crystallized twice from 75 ml. of ethanol and twice from ethyl acetate to yield 1.8 g. of 3-(4-methylpiperazino)-5,6-bis(4-me;thoxyphenyl)-1,2,4-triazine, mp about 158°-160°C.
Workup
- customthe solid product was collected
- customThe product was crystallized twice from 75 ml
- customof ethanol and twice from ethyl acetate to yield 1.8 g
Sources & evidence
- ORD record
- ord-2df90fefbdf4405a9553b52754072f6d
- Source dataset
- uspto-grants-1976_09
- Patent number
- US03979516
Reaction notes
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