2-(3-nitroanilino)-2-oxoacetic acid → HCID 69099830, compound
Reaction equation
[F:1][C:2]1[CH:14]=[CH:13][C:5]([CH2:6][CH:7]2[CH2:12][CH2:11][NH:10][CH2:9][CH2:8]2)=[CH:4][CH:3]=1.[N+:15]([C:18]1[CH:19]=[C:20]([NH:24][C:25](=[O:29])[C:26](O)=[O:27])[CH:21]=[CH:22][CH:23]=1)([O-:17])=[O:16]>C(OCC)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][CH:7]2[CH2:8][CH2:9][N:10]([C:26](=[O:27])[C:25]([NH:24][C:20]3[CH:21]=[CH:22][CH:23]=[C:18]([N+:15]([O-:17])=[O:16])[CH:19]=3)=[O:29])[CH2:11][CH2:12]2)=[CH:13][CH:14]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is prepared from 4-(4-fluoro-benzyl)-piperidine and N-(3-nitro-phenyl)-oxalamic acid (Example 10a according to the method described in Example 2. Melting Point: 135-138° C. (diethylether)
Sources & evidence
- ORD record
- ord-a477cb3e70174e7e80fb9ac5d9ecb3c0
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435744B2
Reaction notes
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