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Chemical Structure| 94205-21-7 Chemical Structure| 94205-21-7

Structure of 94205-21-7

Chemical Structure| 94205-21-7

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Product Details of [ 94205-21-7 ]

CAS No. :94205-21-7
Formula : C16H10ClNO3
M.W : 299.71
SMILES Code : O=C(C1=C(C2=CC=CC=C2)C3=C(NC1=O)C=CC(Cl)=C3)O
MDL No. :MFCD26131164

Safety of [ 94205-21-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 94205-21-7 ]

* 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 [ 94205-21-7 ]

[ 94205-21-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 35661-51-9 ]
  • [ 94205-21-7 ]
  • [ 1433903-58-2 ]
YieldReaction ConditionsOperation in experiment
102 mg A mixture of 6-chloro-2-oxo-4-phenyl-l,2-dihydro-quinoline-3-carboxylic acid (100 mg, 334 ?????, Eq: 1.00) and phosphorus oxychloride (3.29 g, 2 ml, 21.5 mmol, Eq: 64.3) was heated to 120°C for 3h. The reaction mixture was evaporated to dryness and the remaining residue was co-evaporated with toluene (2x). The residue was dissolved in DCM (1 ml) and 9-fluorenylmethyl carbazate (127 mg, 500 ?????, Eq: 1.5) was added. The reaction mixture was stirred at RT for 4h. Then water was added and the mixture was extracted with ethyl acetate (3x). The combined extracts were washed with water and brine, dried with Na2S04 and evaporated. The remaining residue was purified by columnchromatography (silica gel, DCM/EtOAc 9: 1) to afford the title compound as off-white solid (102 mg). MS (ESI): 554.1 (M+H)+.
102 mg Step D: N'-(2,6-Dichloro-4-phenyl-quinoline-3-carbonyl)-hydrazinecarboxylic acid 9H-fluoren-9-ylmethyl ester A mixture of 6-chloro-2-oxo-4-phenyl-1,2-dihydro-quinoline-3-carboxylic acid (100 mg, 334 mumol, Eq: 1.00) and phosphorus oxychloride (3.29 g, 2 ml, 21.5 mmol, Eq: 64.3) was heated to 120° C. for 3 h. The reaction mixture was evaporated to dryness and the remaining residue was co-evaporated with toluene (2*). The residue was dissolved in DCM (1 ml) and 9-fluorenylmethyl carbazate (127 mg, 500 mumol, Eq: 1.5) was added. The reaction mixture was stirred at RT for 4 h. Then water was added and the mixture was extracted with ethyl acetate (3*). The combined extracts were washed with water and brine, dried with Na2SO4 and evaporated. The remaining residue was purified by column chromatography (silica gel, DCM/EtOAc 9:1) to afford the title compound as off-white solid (102 mg). MS (ESI): 554.1 (M+H)+.
 

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