HCID 19438785, compound → HCID 19438755, compound

HRID 1733885Notes

Reaction equation

HRID 1733885 reaction equation
F[C:2]1[CH:11]=[C:10]2[C:5]([NH:6][C:7](=[O:16])[C:8]3[N:9]2[C:12](=[O:15])[NH:13][N:14]=3)=[CH:4][C:3]=1[N+:17]([O-:19])=[O:18].[C:20]1([C:26]2[N:27]=[CH:28][NH:29][CH:30]=2)[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[C:20]1([C:26]2[N:27]=[CH:28][N:29]([C:2]3[CH:11]=[C:10]4[C:5]([NH:6][C:7](=[O:16])[C:8]5[N:9]4[C:12](=[O:15])[NH:13][N:14]=5)=[CH:4][C:3]=3[N+:17]([O-:19])=[O:18])[CH:30]=2)[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1

Participants

3

Reactant 2

HCID 19438785HCID 19438785, compoundHCID 178418822HCID 178418822, compound

Product 1

HCID 19438755HCID 19438755, compound

Procedure

The title compound was prepared from 8-fluoro-7-nitro[1,2,4]triazolo[4,3-a]quinoxaline-1,4(2H,5H)-dione and 4-phenylimidazole by a method analogous to the method described in example 11. M.p. 365° C. (decomp.).

Sources & evidence

ORD record
ord-ca086c774f62465dbc935db93ee7e3e8
Source dataset
uspto-grants-1996_07
Patent number
US05532236

Reaction notes

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