4-Chloro-2-(methylsulfanyl)-7-phenylpyrazolo[1,5-a][1,3,5]triazine → HCID 178503494, compound
Reaction equation
[NH2:1][CH2:2][CH2:3][C:4]1[N:8]=[CH:7][NH:6][CH:5]=1.Cl[C:10]1[N:15]2[N:16]=[C:17]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH:18]=[C:14]2[N:13]=[C:12]([S:25][CH3:26])[N:11]=1>>[NH:6]1[CH:5]=[C:4]([CH2:3][CH2:2][NH:1][C:10]2[N:15]3[N:16]=[C:17]([C:19]4[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=4)[CH:18]=[C:14]3[N:13]=[C:12]([S:25][CH3:26])[N:11]=2)[N:8]=[CH:7]1Participants
3
Procedure
4-[4-imidazolylethylamino]-2-methylthio-7-phenylpyrazolo[1,5-a]-1,3,5-triazine is prepared from histamine and 4-chloro-2-methylthio-7-phenylpyrazolo[1,5-a]-1,3,5-triazine according to conventional methods.
Sources & evidence
- ORD record
- ord-a10d06fc729443d2996ee0407b63672f
- Source dataset
- uspto-grants-1986_01
- Patent number
- US04565815
Reaction notes
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