Diglyme → HCID 23459607, compound

HRID 2287147Notes

Reaction equation

HRID 2287147 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]=1

Participants

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

  1. filtrationThe mixture is filtered hot
  2. customevaporated to dryness

Sources & evidence

ORD record
ord-aeba8d20e4184f8a82f9645751ba4d4b
Source dataset
uspto-grants-1981_05
Patent number
US04269836

Reaction notes

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