Hydrazinecarboxylic acid, ethyl ester → HCID 53882320, compound
Reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH:11]=O.[CH2:13]([O:15][C:16](=[O:19])[NH:17][NH2:18])[CH3:14]>CO>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH:11]=[N:18][NH:17][C:16]([O:15][CH2:13][CH3:14])=[O:19]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 3.93 gm (0.025 mole) of 2-quinolinecarboxaldehyde, 2.60 gm (0.025 mole) of ethylcarbazate and 100 ml of methanol is refluxed for 8 hrs. The hot solvent is evaporated in vacuo to give a solid. The crude product is crystallized from ethyl acetate/Skellysolve B to yield 1.19 gm (20%) of the title compound, having a melting point of 163°-165° C.
Workup
- temperatureis refluxed for 8 hrs
- customThe hot solvent is evaporated in vacuo
- customto give a solid
- customThe crude product is crystallized from ethyl acetate/Skellysolve B
Sources & evidence
- ORD record
- ord-42f7745237f342f7898fab889b608753
- Source dataset
- uspto-grants-1989_09
- Patent number
- US04870082
Reaction notes
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