Hydrazine → HCID 12818616, compound
Reaction equation
C([O:3][C:4]([C:6]1[C:7](=[O:19])[N:8]([CH2:17][CH3:18])[C:9]2[C:14]([C:15]=1[NH2:16])=[CH:13][CH:12]=[CH:11][N:10]=2)=O)C.[NH2:20][NH2:21]>C(O)C>[NH2:16][C:15]1[C:14]2[C:9](=[N:10][CH:11]=[CH:12][CH:13]=2)[N:8]([CH2:17][CH3:18])[C:7](=[O:19])[C:6]=1[C:4]([NH:20][NH2:21])=[O:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A stirred mixture of 2 g. of 4-amino-1-ethyl-1,2-dihydro-2-oxo-1,8-naphthyridine-3-carboxylic acid ethyl ester in 20 ml. of ethanol containing 5 ml. of hydrazine was heated under reflux for 4 hours. The mixture was cooled and the insoluble material was collected. The filter cake was recrystallized from ethanol to produce 1.1 g. of product, m.p. 275°-277° C. dec.
Workup
- additionA stirred mixture of 2 g
- temperatureunder reflux for 4 hours
- temperatureThe mixture was cooled
- customthe insoluble material was collected
- customThe filter cake was recrystallized from ethanol
- customto produce 1.1 g
Sources & evidence
- ORD record
- ord-534b1ffc245c49fbb722f10bf230eb50
- Source dataset
- uspto-grants-1982_09
- Patent number
- US04350817
Reaction notes
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