Adenine → HCID 23155315, compound

HRID 1912780Notes

Reaction equation

HRID 1912780 reaction equation
[N:1]1[C:9]([NH2:10])=[C:8]2[C:4]([N:5]=[CH:6][NH:7]2)=[N:3][CH:2]=1.[F:11][C:12]1[CH:17]=[C:16](F)[CH:15]=[CH:14][C:13]=1[N+:19]([O-])=O.[Cl:22][C:23]1[CH:28]=[CH:27][C:26]([N:29]=[C:30]=[O:31])=[CH:25][C:24]=1[C:32]([F:35])([F:34])[F:33]>>[ClH:22].[NH2:10][C:9]1[N:1]=[CH:2][N:3]=[C:4]2[C:8]=1[N:7]=[CH:6][N:5]2[C:16]1[CH:15]=[CH:14][C:13]([NH:19][C:30]([NH:29][C:26]2[CH:27]=[CH:28][C:23]([Cl:22])=[C:24]([C:32]([F:34])([F:33])[F:35])[CH:25]=2)=[O:31])=[C:12]([F:11])[CH:17]=1

Participants

4

Reactant 3

HCID 190AdenineHCID 679672,4-DifluoronitrobenzeneHCID 27332651-Chloro-4-isocyanato-2-(trifluoromethyl) benzene

Product 1

HCID 23155315HCID 23155315, compound

Procedure

The title compound can be synthesized from adenine, 2,4-difluoronitrobenzene and 4-chloro-3-(trifluoromethyl)phenyl isocyanate by the same method as in Examples 29 and 30.

Sources & evidence

ORD record
ord-e1928703b3904f31a20120a426a16169
Source dataset
uspto-grants-2013_12
Patent number
US08609656B2

Reaction notes

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