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Chemical Structure| 417721-35-8 Chemical Structure| 417721-35-8

Structure of 417721-35-8

Chemical Structure| 417721-35-8

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Product Details of [ 417721-35-8 ]

CAS No. :417721-35-8
Formula : C11H7Cl2NO2
M.W : 256.08
SMILES Code : O=C(Cl)C1=C(OC)C=C2N=CC=C(Cl)C2=C1

Safety of [ 417721-35-8 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314-H290
Precautionary Statements:P501-P260-P234-P264-P280-P390-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P406-P405
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 417721-35-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 417721-35-8 ]

[ 417721-35-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 417721-35-8 ]
  • [ 417721-36-9 ]
YieldReaction ConditionsOperation in experiment
With ammonia; In tetrahydrofuran; water; at 0 - 20℃; for 0.5h; To 7-methoxy-4-oxo-1,4-dihydroquinoline-6-carboxylic acid (2.0 g) were added thionyl chloride (10 mL) and a small amount of N,N-dimethylformamide, and the mixture was heated under reflux for 2 hours. The mixture was concentrated under vacuum, followed by azeotropic distillation twice with toluene to give 7-methoxy-4-chloro-quinoline-6-carbonyl chloride (2.7 g). Subsequently, 7-methoxy-4-chloro-quinoline-6-carbonyl chloride (2.7 g) thus obtained was dissolved in tetrahydrofuran (150 mL), and the solution was cooled to 0° C. 30percent aqueous ammonia (5 mL) was added thereto, and the mixture was stirred at room temperature for 30 minutes. Water was added thereto, and the resultant mixture was extracted three times with ethyl acetate. The combined organic phase was washed with water and saturated brine, dried over sodium sulfate, and dried under vacuum to give the titled compound (1.35 g). 1H-NMR (DMSO-d6): 4.03 (3H, s), 7.56-7.66 (2H, m), 7.79 (1H, brs), 7.88 (1H, brs), 8.46-8.49 (1H, m), 8.78-8.82 (1H, m).
With ammonia; In dichloromethane; for 0.0833333h; Under an atmosphere of argon, oxalyl chloride (1 ml) was added to a stirred suspension of 4-chloro-7-methoxyquinoline-6-carboxylic acid (2.5 g) in methylene chloride (40 ml) and the mixture was stirred at ambient temperature for 10 minutes. Diisopropylethylamine (2 ml)I5 was added and the mixture was stirred at ambient temperature for 10 minutes. Ammonia gas was bubbled through the resultant solution for 5 minutes. The mixture was partitioned between methylene chloride and water. A precipitated solid was isolated by filtration. The organic phase was washed with brine, dried over magnesium sulphate and evaporated. The residue together with the precipitated solid was purified by column chromatography on silica20 using a solvent gradient of 100:0 to 4:1 of methylene chloride and methanol as eluent. There was thus obtained 4-chloro-7-methoxyquinoline-6-carboxamide (1.26 g); 1H NMR: (DMSOd6) 4.04 (s, 3H), 7.6 (s, IH), 7.66 (d, IH), 7.81 (br s, IH), 7.91 (br s, IH), 8.5 (s, IH), 8.81 (d, IH); Mass Spectrum: M+H+ 237 and 239.
With ammonium hydroxide; In dichloromethane; at 0 - 25℃; for 0.5h; Compound ID (300.00 g, 1.17 mol) was dissolved in dichloromethane (750.00 ml) and added to aqueous ammonia (1.03 kg, 5.85 mol), and the ice bath was controlled at 0-5°C. The reaction solution was stirred at 25°C for half an hour. The completion of the reaction was detected by TLC. The turbid liquid was then filtered. The solid was washed with water(50 ml) and then dried. The filtrate was extracted with a mixture of dichloromethane and isopropanol (3: 1, 100 ml * 3) and dried. The organic phase was washed with a NaCl solution (50 ml), dried over sodium sulfate and then was dryed by a water pump. The residue was beaten with a mixture of methylene chloride and ethyl acetate (1: 1, 20 ml) for 15 hours and then filtered and spin-dried. Compound IE (176.00 g, 669.34 mmol, the yield was 57.21percent, and the purity was 90percent) was obtained as a gray solid. 1H NMR (400 MHz, DMSO-d6) ppm 4.02 (s, 3 H) 7.58 (s, 1 H) 7.64 (d, J=4.77 Hz, 1 H) 7.77 - 7.93 (m, 2 H) 8.48 (s, 1 H) 8.81 (d, J=5.02 Hz, 1 H)
  • 2
  • [ 417721-35-8 ]
  • ammonium hydroxide [ No CAS ]
  • [ 417721-36-9 ]
YieldReaction ConditionsOperation in experiment
In tetrahydrofuran; water; Production Example 152-3 7-Methoxy-4-chloroquinoline-6-carboxamide 7-Methoxy-4-chloroquinoline-6-carbonyl chloride (2.7 g) was dissolved in tetrahydrofuran (150 ml), and the solution was cooled to 0° C. After adding 30percent ammonia water (5 ml), the mixture was stirred at room temperature for 30 minutes. Water was added, extraction was performed 3 times with ethyl acetate, and then the organic layers were combined, washed with water and saturated brine, dried over sodium sulfate and dried under reduced pressure to obtain the title compound (1.35 g). 1H-NMR Spectrum (DMSO-d6) delta (ppm): 4.03 (3H, s), 7.56-7.66 (2H, m), 7.79 (1H, brs), 7.88 (1H, brs), 8.46-8.49 (1H, m), 8.78-8.82 (1H, m)
 

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