Nitric Acid → HCID 22098195, compound
Reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][C:12]([N:15]3[CH2:19][CH2:18][N:17]([CH2:20][CH2:21][C:22]([O:24][CH3:25])=[O:23])[C:16]3=[O:26])=[CH:11][CH:10]=2)=[CH:5][CH:4]=1)#[N:2].[N+:27]([O-])([OH:29])=[O:28]>>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([C:9]2[CH:10]=[CH:11][C:12]([N:15]3[CH2:19][CH2:18][N:17]([CH2:20][CH2:21][C:22]([O:24][CH3:25])=[O:23])[C:16]3=[O:26])=[C:13]([N+:27]([O-:29])=[O:28])[CH:14]=2)=[CH:7][CH:8]=1)#[N:2]Participants
3
Procedure
Prepared by reacting 1-(4'-cyano-4-biphenylyl)-3-(2-methoxycarbonyl-ethyl)-imidazolidin-2-one with fuming nitric acid at 0° C.
Workup
- customPrepared
- customat 0° C.
Sources & evidence
- ORD record
- ord-2abbb3dc368e447d88ed78b0624dc5ba
- Source dataset
- uspto-grants-1995_12
- Patent number
- US05478942
Reaction notes
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