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Chemical Structure| 2037-31-2 Chemical Structure| 2037-31-2

Structure of 2037-31-2

Chemical Structure| 2037-31-2

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Product Details of [ 2037-31-2 ]

CAS No. :2037-31-2
Formula : C6H5ClS
M.W : 144.62
SMILES Code : SC1=CC=CC(Cl)=C1
MDL No. :MFCD00004839

Safety of [ 2037-31-2 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P280-P305+P351+P338-P310
Class:8
UN#:1760
Packing Group:

Application In Synthesis of [ 2037-31-2 ]

* 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 [ 2037-31-2 ]

[ 2037-31-2 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 53595-65-6 ]
  • [ 2037-31-2 ]
  • [ 63031-86-7 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; In water; N,N-dimethyl-formamide; at 130 - 150℃; for 0.75h;Microwave irradiation; INTERMEDIATE 29; This shows the preparation of 5-[(3-chlorophenyl)thio]thiophene-2-sulfonamide,To a solution of 3-chlorobenzenethiol (87 mg) and 5-bromothiophene-2-sulfonamide (121 mg) in DMF (1 mL) was added aqueous 2 N sodium hydroxide solution (100 μL) and water (1 mL). The reaction was heated in a CEM Discover microwave for 15 rain at 130 C, then for a further 30 min at 150 C. The dark solution was partitioned between diethyl ether and water, and the organic phase was dried over sodium sulfate and concentrated in vacuo. The crude residue was purified by RPHPLC (Xterra, 5% to 95% acetonitrile in TFA (0.2% aq.)) to give the title compound 5-[(3- chlorophenyl)thio]thiophene-2-sulfonamide (35 mg).1H NMR (300 MHz, DMSO) δ 7.79 (s, 2H), 7.56 (d, 1H), 7.47 (d, 1H), 7.44 - 7.35 (m, 3H), 7.30 - 7.26 (m, 1H).
  • 2
  • [ 2037-31-2 ]
  • [ 116986-13-1 ]
  • [ 126570-66-9 ]
YieldReaction ConditionsOperation in experiment
With sodium methylate; In methanol; A. 2-CYANO-3-(3-CHLOROPHENYLTHIOMETHYL)PYRIDINE STR45 To a stirred, cloudy solution of sodium methoxide (14.7 g, 0.27 mol) in methanol (450 mL), contained in a water bath, add a solution of 3-chlorothiophenol (39.5 g, 0.27 mol) in methanol (95 mL). To the resultant solution add a solution of <strong>[116986-13-1]2-cyano-3-(bromomethyl)pyridine</strong> (48.9 g, 0.25 mol) in methanol (195 mL), and stir the reaction mixture at room temperature for 1 h. Concentrate the reaction mixture under reduced pressure, add 500 mL of ether to the residue, stir, and filter to remove the sodium bromide. Evaporate ether under reduced pressure to obtain the title compound as an amber oil, which may be used without further purification.
With sodium methylate; In methanol; B. 2-Cyano-3-(3-chlorophenylthiomethyl)pyridine STR80 To a stirred, cloudy solution of sodium methoxide (14.7 g, 0.27 mol) in methanol (450 mL), contained in a water bath, add a solution of 3-chlorothiophenol (39.5 g, 0.27 mol) in methanol (95 mL). To the resultant solution add a solution of the title compound of Part A above (48.9 g, 0.25 mol) in methanol (195 mL), and stir the reaction mixture at room temperature for 1 h. Concentrate the reaction mixture under reduced pressure, add 500 mL of ether to the residue, stir, and filter to remove sodium bromide. Evaporate ether under reduced pressure to obtain the title compound as an amber oil, which may be used without further purification in the following ring-closure process (Part C).
  • 3
  • [ 2037-31-2 ]
  • [ 34667-88-4 ]
  • C13H7ClN2O2S [ No CAS ]
  • 4
  • [ 2037-31-2 ]
  • [ 163622-50-2 ]
  • 5-((3-chlorophenyl)thio)-7H-pyrrolo[2,3-d]pyrimidin-4-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
15.7% With copper(l) iodide; potassium carbonate; In ethylene glycol; isopropyl alcohol; at 130℃; for 2.0h;Inert atmosphere; Example 10: 5-((3-chlorophenyl)thio)-7H-pyrrolo[2,3-d]pyrimidin-4-aminemine. [0828] Process C: . Synthesis proceeds via Ullman coupling. To a 20mL argon purged scintillation vial with magnetic stir bar is added intermediate I8 (150mg, (1497) 0.577mmol), 3-chlorobenzenethiol (67uL, 0.557mmol), copper iodide (5.6mg, 0.029mmol), potassium carbonate (206mg, 1.49mmol), 2-propanol (1322uL, 17.3mmol), and ethylene glycol (166uL, 3mmol). Reaction is heated to 130C for 1 hour and then cooled to room temperature for one hour. Purification by HPLC using acetonitrile- water in the presence of 0.1% formic acid yields intermediate 5-((3-chlorophenyl)thio)-7H-pyrrolo[2,3-d]pyrimidin-4-aminemine (25.1mg, 15.7%). LC-MS (ES+) calcd for C12H9ClN4S (M+H)+ 277.02, found 277.40.
 

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