HCID 1531802, compound → HCID 57720100, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:15](=[O:16])[C:14]2[C:9]3=[C:10]([CH2:17][CH2:18][CH2:19][N:8]3[CH:7]=1)[CH:11]=[CH:12][CH:13]=2)=[O:5])[CH3:2].OS(O)(=O)=O.[N+:25]([O-])([OH:27])=[O:26]>>[CH2:1]([O:3][C:4]([C:6]1[C:15](=[O:16])[C:14]2[C:9]3=[C:10]([CH2:17][CH2:18][CH2:19][N:8]3[CH:7]=1)[CH:11]=[CH:12][C:13]=2[N+:25]([O-:27])=[O:26])=[O:5])[CH3:2]Participants
3
Conditions
- Temperature
- 0 °C
Procedure
1-Oxo-6,7-dihydro-1H,5H-pyrido[3,2,1-ij]quinoline-2-carboxylic acid ethyl ester (1.0 g) was placed in round bottom flask and to that, mixture of H2SO4/HNO3 (1:1) was added and stirred for 3 hours at 0° C. The reaction mixture was poured on ice and precipitate was filtered off affording 900 mg of title product (LC/MS: 95%).
Workup
- additionwas added
- additionThe reaction mixture was poured on ice and precipitate
- filtrationwas filtered off
Sources & evidence
- ORD record
- ord-954a16f0c0cf480884bf88843454c761
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07547679B2
Reaction notes
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