Diglyme → HCID 23459607, compound
Reaction equation
C([N:7]1[N:11]2[C:12]3[C:26]4[CH:27]=[N:28][NH:29][C:25]=4[N:24]=[CH:23][C:13]=3[C:14](=[O:22])[N:15]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[C:10]2=[N:9][CH2:8]1)C1OC=CC=1.COCCOCCOC.[Se](=O)=O>>[C:16]1([N:15]2[C:14](=[O:22])[C:13]3[CH:23]=[N:24][C:25]4[NH:29][N:28]=[CH:27][C:26]=4[C:12]=3[N:11]3[N:7]=[CH:8][N:9]=[C:10]23)[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1Participants
4
Procedure
0.01 mol. of 1-furfuryl-4-phenyl-4H-pyrazolo[4',3':5,6]pyrido[3,4-e][1,2,4]triazolo[1,5-a]pyrimidin-5(8H)-one is heated in 50 ml. of diethyleneglycol dimethylether containing 0.01 mol. of selenium dioxide at reflux temperature with stirring for two hours. The mixture is filtered hot and evaporated to dryness. 4-Phenyl-4H-pyrazolo[4',3':5,6]pyrido[3,4-e][1,2,4]triazolo[1,5-a]-pyrimidin-5(8H)-one remains.
Workup
- filtrationThe mixture is filtered hot
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-aeba8d20e4184f8a82f9645751ba4d4b
- Source dataset
- uspto-grants-1981_05
- Patent number
- US04269836
Reaction notes
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