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Chemical Structure| 276863-95-7 Chemical Structure| 276863-95-7

Structure of 276863-95-7

Chemical Structure| 276863-95-7

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Product Details of [ 276863-95-7 ]

CAS No. :276863-95-7
Formula : C13H11ClN2O
M.W : 246.69
SMILES Code : ClCCCC(=O)C1=CNC2=C1C=C(C=C2)C#N
MDL No. :MFCD09833260

Safety of [ 276863-95-7 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H331-H341
Precautionary Statements:P201-P202-P261-P264-P270-P271-P280-P302+P352-P304+P340-P308+P313-P310-P330-P361-P403+P233-P405-P501
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 276863-95-7 ]

* 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 [ 276863-95-7 ]

[ 276863-95-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 276863-95-7 ]
  • [ 183288-46-2 ]
  • vilazodone N-oxide [ No CAS ]
YieldReaction ConditionsOperation in experiment
85% With triethylamine; potassium iodide; In N,N-dimethyl-formamide; at 20 - 90℃; for 49h;Inert atmosphere; 3-(4-chlorobutyryl)-1H-indole-5-carbonitrile (VIII) (95g, 0.41mol, 1.0eq),5- (piperazin-1-yl) benzofuran-2-carboxamide (II) (100 g, 0.41 mol.KI (6.8 g, 0.041 mol, 0.1 eq),TEA (226 ml, 4.0 eq)And DMF (1 L) were added to a 2 L three-necked flask,Stirring under vacuum degassing 2min, nitrogen replacement,So three times.The reaction solution was stirred at room temperature for 1 hour,The temperature was then raised to an internal temperature of 85 to 90 C,Reaction for 48 hours,HPLC monitoring of starting material VIII) Residual less than 3%Stop heating,Cool to room temperature.To the reaction solution was added dropwise 1.1 L of water until the white solid precipitated completely,With about 5 hours,filter,The filter cake was beaten with 2 L of water for 1 hour,filter,Vacuum drying,168 g of crude product was obtained.168 g of crude product was added to 3 L of absolute ethanol,Heated to reflux dissolved,While hot filter,The filtrate slowly cooled to room temperature crystallization.filter,Filter cake with 350ml anhydrous ethanol beating 30min,filter,160g vacuum drying to give white crystals of intermediate (IX) compound.Yield: 85%, purity 99.9% (HPLC)
7.0% With tributyl-amine; In 1-methyl-pyrrolidin-2-one; at 25 - 130℃; for 24h; 5-(Piperazin-l-yl)-l-benzofuran-2-carboxamide of Formula V (10.0 g) and 3-(4- chlorobutanoyl)-lH-indole-5-carbonitrile of Formula VI (11.1 g) were added to N-methyl pyrrolidone (50 mL), followed by the addition of tributyl amine (7.6 g) at 25C to 30C. The reaction mixture was stirred at 120C to 130C for 24 hours. The reaction mixture was cooled to 25C to 30C. 2-Propanol (100 mL) and 2-propanolic hydrochloric acid solution (15 mL; 20%) were added to the reaction mixture at 25C to 30C. The reaction mixture was stirred for 1 hour, filtered, washed with 2-propanol (20 mL), and then washed with methanol (20 mL) to obtain the crude oxo vilazodone (9.5 g). The crude oxo vilazodone obtained (2 g) was purified by passing it through a YMC-Pack ODS-A, 15 mupiiota, 500 mm x 30 mm column at ambient temperature, using a mixture of 0.5 M KH2PO4 buffer and acetonitrile (60:40% v/v ratio; 5000 mL) as the mobile phase, followed by adjusting the pH of the solution to 7.5 ± 0.05 with 10% aqueous ammonia solution (0.2 mL; prepared by dissolving 1 mL of 25% ammonia solution in 10 mL water) to obtain the oxo vilazodone impurity of Formula III. Yield: 7.0% NMR (400 MHz, CDC13), delta (in ppm): 2.05 (m, 2H), 2.56 (t, 2H), 2.70 (t, 4H), 3.01 (t, 2H), 3.13 (t, 4H), 7.19 (m, 2H), 7.53 (m, 4H), 8.38 (s, 1H), 8.67 (m, 1H). Mass: 456.4 [M + H]+; MS/MS: 211.1, 169.0. IR in KBr, (in cm"1): 3418 (N-H stretching), 2221 (CN stretching), 1669, 1616 (-C=0 stretchings), 808, 887 (aryl C-H bendings).
 

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