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CAS No. : | 248282-13-5 | MDL No. : | MFCD20268110 |
Formula : | C14H15NO5 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | N/A |
M.W : | 277.27 g/mol | Pubchem ID : | 54728881 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P280-P301+P312-P302+P352-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
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Yield | Reaction Conditions | Operation in experiment |
---|---|---|
50% | In toluene for 6h; Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
47% | In toluene for 6h; Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
82% | In toluene for 6h; Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
80% | In toluene | 1 N-Ethyl-N-phenyl-1,2-dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxamide (Method A) EXAMPLE 1 N-Ethyl-N-phenyl-1,2-dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxamide (Method A) N-Ethylaniline (3.0 g, 25 mmol) was dissolved in 80 ml of toluene and about 30 ml of the solvent was distilled off in order to obtain a dry solution. To this boiling solution was added 1,2-dihydro-4hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxylic acid ethyl ester (2.7 g, 10 mmol). The ethanol formed during the reaction was distilled off together with some toluene for about 4 hours. The reaction mixture was cooled to room temperature. The precipitate was collected, washed with cold toluene and hexane and dried to give the title compound (2.8 g), yield 80%. 1 H NMR (CDCl3) δ 1.26 (3H, t), 3.50 (3H, s), 3.97 (2H, q), 4.03 (3H,s), 6.67 (1H, d), (6.87 (1H, d), 7.12-7.25 (3H, m), 7.36-7.44 (3H, m). 13C NMR (CDCl3) δ 13.0 (CH3), 29.6 (CH3), 43.8 (CH2), 56.8 (CH3), 103.2 (CH), 104.2 (C), 108.3 (CH), 110.5 (C), 127.3 (2CH), 127.4 (CH), 128.5 (2CH), 131.2 (CH), 141.1 (C), 141.9 (C), 156.9 (C), 157.1 (C), 160.2 (C), 164.4 (C). ESI MS/MS [M+H]+ 353, fragments 232 and 122. |
79% | In toluene for 6h; Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
83% | In toluene for 6h; Heating; | |
83% | In toluene for 4h; Heating / reflux; | 7 N-Methylaniline (2.7g, 0.025 mol) was dissolved in 80 ml of toluene and about 30 ml of the solvent was distilled off in order to obtain a dry solution. 1,2-Dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxylic acid ethyl ester (2.7 g, 0.01 mol) was added to the boiling solution. The ethanol formed during the reaction was distilled off together with some toluene for about 4 hours. The mixture was cooled to room temperature. The precipitate was collected, washed with cold toluene and hexane and dried to give the title compound (2.8 g), yield 83 %. 1H NMR (CDCl3) δ 3.49 (3H, s), 3.50 (3H, s), 4.03 (3H, s), 6.66 (1H, d), 6.86 (1H, d), 7.08-7.48 (6H, m). 13C NMR (CDCl3) δ 29.7 (CH3), 36.8 (CH3), 56.8 (CH3), 103.3 (CH), 104.2 (C), 108.4 (CH), 110.2 (C), 126.2 (CH), 127.2 (CH), 128.6 (CH), 131.4 (CH), 141.2 (C), 143.6 (C), 157.0 (C), 157.4 (C), 160.3 (C), 165,1 (C). ESI MS/MS [M+H]+ 339, fragment 232. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
89% | In toluene for 6h; Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With sodium hydride In N,N-dimethyl-formamide at 85℃; for 5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
83% | In toluene for 6h; Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
77% | With hydrogenchloride; acetic anhydride | 9 1,2-Dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxylic acid EXAMPLE 9 1,2-Dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxylic acid While cooling, 10 ml of conc. hydrochloric acid was added to 30 ml of acetic anhydride. To this solution, 1,2-dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxylic acid ethyl ester (10.5 g, 38 mmol) was added and the mixture heated at 80° C. for 14 hours. The mixture was cooled to room temperature and the crystalline product was filtered off, washed with cold methanol and dried to give the title compound (7.2 g), yield 77%. 1H NMR ((CDCl3) δ 3.73 (3H, s) 4.02 (3H, s), 6.82 (1H, d), 7.02 (1H, d), 7.62 (1H, t). |
77% | With hydrogenchloride; acetic anhydride | 6 1,2-Dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxylic acid EXAMPLE 6 1,2-Dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxylic acid While cooling, 10 ml of conc. hydrochloric acid was added to 30 ml of acetic anhydride. To this solution, 1,2-dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxylic acid ethyl ester (10.5 g, 38 mmol) was added and the mixture heated at 80° C. for 14 hours. The mixture was cooled to room temperature and the crystalline product was filtered off, washed with cold methanol and dried to yield the title compound (7.2 g), yield 77%. 1H NMR ((CDCl3) δ 3.73 (3H, s) 4.02 (3H, s), 6.82 (1H, d), 7.02 (1H, d), 7.62 (1H, t). |
77% | With water In acetic anhydride at 80℃; for 14h; | 6 While cooling, 10 ml of conc. hydrochloric acid was added to 30 ml of acetic anhydride. To this solution, 1,2-dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo- quinoline-3-carboxylic acid ethyl ester (10.5 g, 38 mmol) was added and the mixture heated at 80°C for 14 hours. The mixture was cooled to room temperature and the crystalline product was filtered off, washed with cold methanol and dried to yield the title compound (7.2 g), yield 77 %. 1H NMR ((CDCl3) δ 3.73 (3H, s) 4.02 (3H, s), 6.82 (1H, d), 7.02 (1H, d), 7.62 (1H, t). |
With hydrogenchloride In acetic acid at 60℃; for 6h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 3 steps 1: dioxane / 1 h / 20 °C 2: NaH / dimethylformamide / 5 h / 20 °C 3: NaH / dimethylformamide / 5 h / 85 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: HCl / acetic acid / 6 h / 60 °C 2: SOCl2; Et3N / CH2Cl2 / 4.5 h / 0 - 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: HCl / acetic acid / 6 h / 60 °C 2: SOCl2; Et3N / CH2Cl2 / 4.5 h / 0 - 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: HCl / acetic acid / 6 h / 60 °C 2: SOCl2; Et3N / CH2Cl2 / 4.5 h / 0 - 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: HCl / acetic acid / 6 h / 60 °C 2: SOCl2; Et3N / CH2Cl2 / 4.5 h / 0 - 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: HCl / acetic acid / 6 h / 60 °C 2: SOCl2; Et3N / CH2Cl2 / 4.5 h / 0 - 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: HCl / acetic acid / 6 h / 60 °C 2: SOCl2; Et3N / CH2Cl2 / 4.5 h / 0 - 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: HCl / acetic acid / 6 h / 60 °C 2: SOCl2; Et3N / CH2Cl2 / 4.5 h / 0 - 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
83% | In toluene | 7 N-Methyl-N-phenyl-1,2-dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxy-quinoline-3-carboxamide (not included in the claims)(Method A) EXAMPLE 7 N-Methyl-N-phenyl-1,2-dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxy-quinoline-3-carboxamide (not included in the claims)(Method A) N-Methylaniline (2.7 g, 0.025 mol) was dissolved in 80 ml of toluene and about 30 ml of the solvent was distilled off in order to obtain a dry solution. 1,2-Dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxylic acid ethyl ester (2.7 g, 0.01 mol) was added to the boiling solution. The ethanol formed during the reaction was distilled off together with some toluene for about 4 hours. The mixture was cooled to room temperature. The precipitate was collected, washed with cold toluene and hexane and dried to give the title compound (2.8 g), yield 83%. 1H NMR (CDCl3) δ 3.49 (3H, s), 3.50 (3H, s), 4.03 (3H, s), 6.66 (1H, d), 6.86 (1H, d), 7.08-7.48 (6H, m). 13C NMR (CDCl3) δ 29.7 (CH3), 36.8 (CH3), 56.8 (CH3), 103.3 (CH), 104.2 (C), 108.4 (CH), 110.2 (C), 126.2 (CH), 127.2 (CH), 128.6 (CH), 131.4 (CH), 141.2 (C), 143.6 (C), 157.0 (C), 157.4 (C), 160.3 (C), 165,1 (C). ESI MS/MS [M+H]+ 339, fragment 232. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
48% | In water; N,N-dimethyl-formamide | 1 1,2-Dihydro-4-hydroxy-5-methoxy-1-methyl-2-oxo-quinoline-3-carboxylic acid ethyl ester After being carefully dried, the 5-methoxy-N-methyl-isatoic anhydride (20.7 g, 0.10 mol) was added to a solution of sodium diethylmalonate (31 g, 0.17 mol) in 250 ml of anhydrous N,N-dimethylformamide at room temperature. The solution was heated at 100° C. for 3 hours, cooled to room temperature, 250 ml of water was added and the pH adjusted to 4 with conc. hydrochloric acid. The precipitate was collected by filtration and dried in vacuum to give the title compound as pure white crystals (22 g), yield 48%. 1H NMR (CDCl3) δ 1.43 (t, 3H), 3.62 (s, 3H), 3.96 (s, 3H), 4.45 (q, 2H), 6.70 (d, 1H), 6.92 (d, 1H) 7.55 (t, 1H), 13.5 (s, 1H). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Stage #1: sodium diethylmalonate; 5-methoxy-1-methyl-2H-benzo[d][1,3]oxazine-2,4(1H)-dione In N,N-dimethyl-formamide at 20 - 100℃; for 3h; Stage #2: With hydrogenchloride In water; N,N-dimethyl-formamide at 20℃; | 1 To a solution of 2,6-difluorobensonitril (42 g, 0.30 mol) in 150 ml of anhydrous methanol sodium methoxide (17.9 g, 0.33 mol) was slowly added at 30°C. After being heated under reflux for 1 hour, aqueous 40 % methylamine (133 ml, 1.2 mol) was added and the resulting solution refluxed for 4 days. On cooling, a white solid, 2-methoxy-6-(methylamino)benso-nitrile, precipitated which was collected by filtration. The precipitate was dissolved in an aqueous solution of ethylene glycol (500 ml) and potassium hydroxide (14 g). The solution was refluxed at 150°C over night, cooled to room temperature and the pH adjusted to 4 with cone. hydrochloric acid. The anthranilic acid formed was collected by filtration, washed with water (50 ml) and dried under vacuum. The 6-methoxy-N-methyl-anthranilic acid (32 g, 0.18 mol), and sodium bicarbonate (38 g, 0.45 mol) were suspended in 500 ml of 1,4-dioxane. Phosgene (25 ml, 0.45 mol) was slowly added under cooling in an ice bath. The mixture was warmed at 40°C for 1 hour, cooled to 15°C, and then 150 ml of water was added. The isatoic anhydride formed was collected by filtration. After being carefully dried, the 5-methoxy-N-methyl-isatoic anhydride (20.7 g, 0.10 mol) was added to a solution of sodium diethylmalonate (31 g, 0.17 mol) in 250 ml of anhydrous N,N-dimethylformamide at room temperature. The solution was heated at 100°C for 3 hours, cooled to room temperature, 250 ml of water was added and the pH adjusted to 4 with conc. hydrochloric acid. The precipitate was collected by filtration and dried in vacuum to give the title compound as pure white crystals (22 g), yield 48 %. 1H NMR (CDCl3) δ 1.43 (t, 3H), 3.62 (s, 3H), 3.96 (s, 3H), 4.45 (q, 2H), 6.70 (d, 1H), 6.92 (d, 1H), 7.55 (t, 1H), 13.5 (s, 1H). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1.1: sodium hydrogencarbonate / 1,4-dioxane / 1 h / 0 - 40 °C 2.1: N,N-dimethyl-formamide / 3 h / 20 - 100 °C 2.2: 20 °C / pH 4 |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 3 steps 1.1: potassium hydroxide; water / ethylene glycol / 150 °C / Heating / reflux 1.2: 20 °C / pH 4 2.1: sodium hydrogencarbonate / 1,4-dioxane / 1 h / 0 - 40 °C 3.1: N,N-dimethyl-formamide / 3 h / 20 - 100 °C 3.2: 20 °C / pH 4 |
Tags: 248282-13-5 synthesis path| 248282-13-5 SDS| 248282-13-5 COA| 248282-13-5 purity| 248282-13-5 application| 248282-13-5 NMR| 248282-13-5 COA| 248282-13-5 structure
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H371 | May cause damage to organs |
H372 | Causes damage to organs through prolonged or repeated exposure |
H373 | May cause damage to organs through prolonged or repeated exposure |
Environmental hazards | |
Code | Phrase |
H400 | Very toxic to aquatic life |
H401 | Toxic to aquatic life |
H402 | Harmful to aquatic life |
H410 | Very toxic to aquatic life with long-lasting effects |
H411 | Toxic to aquatic life with long-lasting effects |
H412 | Harmful to aquatic life with long-lasting effects |
H413 | May cause long-lasting harmful effects to aquatic life |
H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
Sorry,this product has been discontinued.
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