Ammonium Hydroxide → 6-(1H-imidazol-2-yl)-1H-1,8-naphthyridin-2-one
Reaction equation
N[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[N:5][CH:6]=[C:7]([C:12]3[NH:13][CH:14]=[CH:15][N:16]=3)[CH:8]=2)[N:3]=1.N([O-])=[O:18].[Na+].[OH-].[NH4+]>S(=O)(=O)(O)O.O>[NH:16]1[CH:15]=[CH:14][N:13]=[C:12]1[C:7]1[CH:8]=[C:9]2[C:4](=[N:5][CH:6]=1)[NH:3][C:2](=[O:18])[CH:11]=[CH:10]2Participants
Procedure
To a mixture of 2-amino-6-(2-imidazolyl)-1,8-naphthyridine (211 mg., 1 mmole) in 40% sulphuric acid (2.5 ml.) at 5° C. is added with stirring sodium nitrite (69 mg., 1 mmole). The solution is allowed to warm to room temperature and then heated at 50° C. for 4 hours. The reaction mixture then is cooled to 5° C. and more sodium nitrite (40 mg., 0.57 mmole) added to ensure reaction goes to completion. The mixture then is heated at 50° C. for two hours, cooled to room temperature, diluted with water and neutralized with ammonium hydroxide affording 140 mg. of solid. The product is purified by dissolving in dilute acetic acid (5 ml.), treating the solution with charcoal, and neutralizing the filtered solution with a few drops of ammonium hydroxide. The product (100 mg., 47%) did not melt below 350° C.
Workup
- temperatureheated at 50° C. for 4 hours
- temperatureThe reaction mixture then is cooled to 5° C.
- customreaction
- temperatureThe mixture then is heated at 50° C. for two hours
- temperaturecooled to room temperature
- customThe product is purified
- dissolutionby dissolving in dilute acetic acid (5 ml.)
- additiontreating the solution with charcoal
- customdid not melt below 350° C.
Sources & evidence
- ORD record
- ord-09b58e8d68ee43dea4cd7407b37e7da1
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03993656
Reaction notes
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