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4-methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrile
methyl iodide
ricinin
Conditions | Yield |
---|---|
Stage #1: 4-methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrile With potassium tert-butylate; tetra-(n-butyl)ammonium iodide In tetrahydrofuran at 0℃; Stage #2: methyl iodide In tetrahydrofuran at 20℃; | 90% |
With potassium carbonate In acetonitrile for 10h; Reflux; | 78% |
2,4-Dimethoxy-pyridin-3-carbonitril
ricinin
Conditions | Yield |
---|---|
With methyl iodide at 130℃; for 6h; | 70% |
With methyl iodide at 155℃; |
1,2-dihydro-4-methoxy-1-methyl-2-oxopyridine-3-carboxylic acid
ricinin
Conditions | Yield |
---|---|
With ethylpolyphosphate; ammonia In chloroform 1a) 2 h, b) 80 deg C, 4 h; | 56% |
4-methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrile
dimethyl sulfate
ricinin
Conditions | Yield |
---|---|
With sodium hydroxide at 0℃; | 53% |
2-Chloro-5-cyano-4-methoxy-N-methylpyrid-6-one
ricinin
Conditions | Yield |
---|---|
With sulfuric acid; zinc |
4-methoxypyridine-3-carbonitrile
ricinin
Conditions | Yield |
---|---|
With dimethyl sulfate; benzene Behandeln des Reaktionsprodukts mit K3 in H2O; |
Conditions | Yield |
---|---|
at 120 - 130℃; | |
at 120 - 130℃; im Vakuum; | |
at 120 - 130℃; im Rohr; |
Conditions | Yield |
---|---|
With chloroform |
ricinin
Conditions | Yield |
---|---|
With methyl bromide at 100℃; | |
With dimethyl sulfate; xylene |
diazomethane
4-hydroxy-1-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile
ricinin
Conditions | Yield |
---|---|
In methanol; diethyl ether for 48h; | 120 mg |
1,1-Dicyan-4-(N,N-dimethylamino)-2-methoxybutadien-1,3
ricinin
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 87 percent / methanol / 15 h / Heating 2: 70 percent / CH3I / 6 h / 130 °C View Scheme |
4-methoxy-1-methyl-2-pyridone
ricinin
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1) BuLi / 1) THF, hexane, -78 deg C, 30 min, 2a) -78 deg C, 15 min 2: 56 percent / ethylpolyphosphate, NH3(g) / CHCl3 / 1a) 2 h, b) 80 deg C, 4 h View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 50 percent / 40percent aq. NaOH, triethylbenzylammonium bromide / benzene / 96 h / 70 °C 2: 1) BuLi / 1) THF, hexane, -78 deg C, 30 min, 2a) -78 deg C, 15 min 3: 56 percent / ethylpolyphosphate, NH3(g) / CHCl3 / 1a) 2 h, b) 80 deg C, 4 h View Scheme |
Conditions | Yield |
---|---|
With 1,4-diaza-bicyclo[2.2.2]octane In N,N-dimethyl-formamide at 90℃; for 6h; Green chemistry; chemoselective reaction; | 92% |
With water; sodium hydroxide In tetrahydrofuran at 110℃; for 2h; | 87.5% |
With sodium hydroxide In water for 0.333333h; | |
With sodium hydroxide for 0.5h; Heating; | 0.31 g |
ricinin
Conditions | Yield |
---|---|
With N-Bromosuccinimide; trifluoroacetic acid In acetonitrile for 8h; Reflux; | 81% |
With bromine In dichloromethane at 60℃; for 48h; | 47.3% |
With bromine In dichloromethane at 60℃; for 48h; |
ricinin
Conditions | Yield |
---|---|
With sulfuric acid at 80 - 90℃; for 6h; | 72% |
With polyphosphoric acid at 110℃; for 2h; | 43.6% |
Conditions | Yield |
---|---|
bei der Zinkstaub-Destillation; |
ricinin
2-Chloro-5-cyano-4-methoxy-N-methylpyrid-6-one
Conditions | Yield |
---|---|
With chlorine; acetic acid |
ricinin
1-methyl-1H-pyridine-2,4-dione
Conditions | Yield |
---|---|
With hydrogenchloride at 140℃; |
ricinin
4-methoxy-1-methyl-2-pyridone
Conditions | Yield |
---|---|
With sulfuric acid |
ricinin
Conditions | Yield |
---|---|
With aqueous alkali | |
With potassium hydroxide | |
With potassium carbonate |
ricinin
Conditions | Yield |
---|---|
With water; bromine | |
With chloroform; bromine |
ricinin
Conditions | Yield |
---|---|
With hydrogenchloride; platinum |
Conditions | Yield |
---|---|
beim Erhitzen auf Dunkelrotglut; |
Conditions | Yield |
---|---|
at 140℃; im Rohr; |
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