1H-Imidazole, 2-(1-methylethyl)- → HCID 19438791, compound

HRID 1733887Notes

Reaction equation

HRID 1733887 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].[CH:20]([C:23]1[NH:24][CH:25]=[CH:26][N:27]=1)([CH3:22])[CH3:21]>>[CH:20]([C:23]1[N:24]([C:2]2[CH:11]=[C:10]3[C:5]([NH:6][C:7](=[O:16])[C:8]4[N:9]3[C:12](=[O:15])[NH:13][N:14]=4)=[CH:4][C:3]=2[N+:17]([O-:19])=[O:18])[CH:25]=[CH:26][N:27]=1)([CH3:22])[CH3:21]

Participants

3

Reactant 2

HCID 1234571H-Imidazole, 2-(1-methylethyl)-HCID 19438785HCID 19438785, compound

Product 1

HCID 19438791HCID 19438791, 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 2-isopropylimidazole by a method analogous to the method described in example 11. M.p. 240° C. decomp.

Sources & evidence

ORD record
ord-14b7728473714354b22e9c687e0f0d52
Source dataset
uspto-grants-1996_07
Patent number
US05532236

Reaction notes

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