Reaction equation
[N-:1]=[N+]=[N-].Cl.[O:5]=[C:6]1[C:11](C(NN)=O)=[CH:10][C:9]([C:16]2[CH:21]=[CH:20][N:19]=[CH:18][CH:17]=2)=[N:8][NH:7]1.N([O-])=O.[Na+].Cl.O=C1C(C(N=[N+]=[N-])=O)=CC(C2C=CN=CC=2)=NN1>O>[NH2:1][C:11]1[C:6](=[O:5])[NH:7][N:8]=[C:9]([C:16]2[CH:21]=[CH:20][N:19]=[CH:18][CH:17]=2)[CH:10]=1Participants
Reactant 5
Product 1
Reagents, catalysts & solvents 1
Procedure
The above procedure of Example G-1 first procedes through the acid azide as seen by the following isolation of the acid azide as its monohydrochloride: To a solution chilled in an ice bath and containing 3.0 g. of 2,3-dihydro-3-oxo-6-(4-pyridinyl)-4-pyridazinecarboxylic acid hydrazide and 60 ml. of 6 N hydrochloric acid was added dropwise with stirring a solution containing 3.0 g. of sodium nitrite in 10 ml. of water over a 30 minute period. The reaction mixture was then stirred for an additional 1 hour, allowing the reaction mixture to warm up to room temperature. The separated solid was collected, washed with water and dried in a vacuum oven over P2O5 at 25° C. for 48 hours to yield 3.0 g. of 2,3-dihydro-3-oxo-6-(4-pyridinyl)-4-pyridazinecarboxylic acid azide monohydrochloride, m.p. >300° C.
Workup
- temperatureTo a solution chilled in an ice bath
- additioncontaining 3.0 g
- additioncontaining 3.0 g
- stirringThe reaction mixture was then stirred for an additional 1 hour
- customThe separated solid was collected
- washwashed with water
- dry with materialdried in a vacuum oven over P2O5 at 25° C. for 48 hours
- customto yield 3.0 g
Sources & evidence
- ORD record
- ord-61b597167197461d9dc9e6fb0ce0906e
- Source dataset
- uspto-grants-1982_08
- Patent number
- US04346221
Linked notes
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