Purine → HCID 22411330, compound
Reaction equation
[N:1]1[CH:9]=[C:8]2[C:4]([N:5]=[CH:6][NH:7]2)=[N:3][CH:2]=1.F[C:11]1[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][CH:12]=1>>[N:7]1([C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][CH:12]=2)[C:8]2[CH:9]=[N:1][CH:2]=[N:3][C:4]=2[N:5]=[CH:6]1Participants
3
Procedure
Prepared from purine and 1-fluoro-4-nitrobenzene as described for Example 1, Step 1. The product precipitated from the reaction mixture as a single isomer; δ (D6 -DMSO) 8.16 (2H, d, J=9.0Hz, Ar--H), 8.48 (2H, d, J=9.0Hz, Ar--H), 9.13 (1H, s, Ar--H), 9.28 (1H, s, Ar--H), 9.39 (1H, s, Ar--H).
Workup
- customThe product precipitated from the reaction mixture as a single isomer
Sources & evidence
- ORD record
- ord-0d0d4a8fa4e9499fad38a995907dc013
- Source dataset
- uspto-grants-1996_05
- Patent number
- US05514682
Reaction notes
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