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Chemical Structure| 17688-68-5 Chemical Structure| 17688-68-5

Structure of 17688-68-5

Chemical Structure| 17688-68-5

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Product Details of [ 17688-68-5 ]

CAS No. :17688-68-5
Formula : C10H13NO2S
M.W : 211.28
SMILES Code : O=S1(CCN(C2=CC=CC=C2)CC1)=O
MDL No. :MFCD00100136

Safety of [ 17688-68-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P501-P270-P264-P301+P312+P330

Application In Synthesis of [ 17688-68-5 ]

* 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 [ 17688-68-5 ]

[ 17688-68-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 17688-68-5 ]
  • [ 33513-42-7 ]
  • [ 27913-96-8 ]
YieldReaction ConditionsOperation in experiment
To a clean, dry 500 mL flask equipped with a heating mantle and addition funnel were added 200 mL of DMF and 50.7 g of N-phenylthiomorpholine-S,S-dioxide (0.2 mol, available from Eastman Chemical Company). The reaction vessel was purged with nitrogen and 20.5 mL of phosphorus oxychloride (0.2 mol) were added at such a rate to keep the temperature from exceeding 35 C. The reaction vessel was heated to 80-90 C. and stirred for about 4 h. The reaction mixture was allowed to cool to room temperature and poured into a mechanically stirred ice water mixture (1 L) containing 100 mL of concentrated ammonium hydroxide. A white precipitate formed that was collected by suction filtration and washed with water. The cake was allowed to dry on the filter overnight to give 54.4 g of product.
With trichlorophosphate; for 4h;Heating; To a mixture of compound 22_1 (500 mg, 1.11 mmol, 1 eq) in AcOH (6.00 mL) was added methylhydrazine (100 mg, 2.17 mmol, 114 mL, 1.96 eq). The mixture was stirred at 85 C for 8 hours. LCMS showed compound 22_1 was consumed and a main peak with the desired mass was detected. The crude was purified by preparative HPLC (column Waters Xbridge 150 x 50 mm,10 mm; mobile phase (0.05% NH4OH) A - water, B - ACN; gradient 8-38% B, 11.5 min) and adjusted pH to 7-8 with saturated NaHCO3aqueous solution. The mixture was extracted with DCM (30 mL x 3). The combined organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to give Cpd 22 (6.00 mg, 15.2 mmol, 1.38% yield, 98.9% purity) as off-white solid. LCMS: product RT = 0.798 min, m/z = 390.1 (M+1)+.HPLC: product RT = 2.004 min.1H NMR: 400 MHz, DMSO-d6: d = 12.41 (br s, 1H), 8.92 (s, 1H), 8.17 (d, J = 4.4 Hz, 1H), 7.68 (br d, J = 2.0 Hz, 1H), 7.54 (d, J = 8.8 Hz, 0.5H), 7.49 - 7.33 (m, 1H), 7.27 (br d, J = 8.8 Hz, 0.5H), 6.82 - 6.67 (m, 2H), 6.54 (s, 1H), 6.26 (br d, J = 7.2 Hz, 1H), 3.85 (s, 3H), 3.64 (s, 3H), 2.09 (s, 3H).
 

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