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Chemical Structure| 204387-54-2 Chemical Structure| 204387-54-2

Structure of 204387-54-2

Chemical Structure| 204387-54-2

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Product Details of [ 204387-54-2 ]

CAS No. :204387-54-2
Formula : C12H16N2O3S
M.W : 268.33
SMILES Code : N#C[C@H]1NCCC1.O=S(C2=CC=C(C)C=C2)(O)=O
MDL No. :MFCD12827848
InChI Key :ZILVRYHBTINJDJ-ZSCHJXSPSA-N
Pubchem ID :87797239

Safety of [ 204387-54-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 204387-54-2 ]

* 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 [ 204387-54-2 ]

[ 204387-54-2 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 104-15-4 ]
  • [ 228244-04-0 ]
  • [ 204387-54-2 ]
YieldReaction ConditionsOperation in experiment
75% In water; acetonitrile; for 24h; General procedure: A solution of compound 3 (10.0 g, 50.96 mmol) in CH3CN (50 mL) was added 4-methylbenzenesulfonic acid hydrate (14.54 g, 76.43 mmol) and stirred at room temperature for 24 h. After the reaction completed, the solution was removed in vacuo. The residual white solid was dissolved in EtOAc (100 mL) and put into fridge overnight, the product 4 (10.3 g, 75%) was precipitated as a white needle crystal. 1H NMR (300 MHz, CD3OD) delta 7.77 (d, J = 7.8 Hz, 2H), 7.20 (d, J = 8.1 Hz, 2H), 4.76-4.75 (m, 1H), 3.51-3.50 (m, 2H), 2.38 (s, 3H), 2.34-2.31 (m, 1H), 2.17-2.09 (m, 2H), 1.90-1.87 (m, 1H). MS (ESI) m/z 97 [M+H]+
75% In acetonitrile; at 20℃; for 24h; A solution of compound 10 (10.0 g, 50.96mmol) in CH3CN (50 mL) was added 4-methylbenzenesulfonic acidhydrate (14.54 g, 76.43mmol) and stirred at room temperature for 24 h. After the reaction completed,the solution was removed in vacuo.The residual white solid was dissolved in EtOAc (100 mL) and put into fridgeovernight, the product 11 (10.3 g, 75%) was precipitated as a white needlecrystal. 1H NMR (CD3OD, 300 MHz): delta 7.77 (d, J = 7.8 Hz, 2H), 7.20 (d, J= 8.1 Hz, 2H), 4.76-4.75 (m, 1H), 3.51-3.50 (m, 2H), 2.38 (s, 3H), 2.34-2.31(m, 1H), 2.17-2.09 (m, 2H), 1.90-1.87 (m, 1H). MS (ESI) m/z 97[M+H]+.
  • 2
  • [ 204387-54-2 ]
  • [ 114873-00-6 ]
  • C19H24FN3O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
General procedure: (S)-2-((tert-Butoxycarbonyl)amino)-3-phenylpropanoic acid (compound 5a, 203.6 mg, 0.768 mmol) in DMF (5 mL) was added HOBt (283.2 mg, 2.10 mmol) and EDCI (257.8 mg, 1.396 mmol). After stirring for 30 min compound 4 (187.2 mg, 0.698 mmol) and additional TEA (0.30 mL, 2.10 mmol) were added. This solution was allowed to stir at room temperature for 20 h and then the saturated NaHCO3 was added. The mixture was extracted with EtOAc and washed with saturated NaCl, dried over Na2SO4 and concentrated. The residue was purified with flash chromatography on silica gel, eluted with a mixture of PE/EA (4/1, v/v) to afford 6a (130 mg, 54%) as a white solid.
  • 3
  • [ 204387-54-2 ]
  • [ 114873-01-7 ]
  • C19H24FN3O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
General procedure: (S)-2-((tert-Butoxycarbonyl)amino)-3-phenylpropanoic acid (compound 5a, 203.6 mg, 0.768 mmol) in DMF (5 mL) was added HOBt (283.2 mg, 2.10 mmol) and EDCI (257.8 mg, 1.396 mmol). After stirring for 30 min compound 4 (187.2 mg, 0.698 mmol) and additional TEA (0.30 mL, 2.10 mmol) were added. This solution was allowed to stir at room temperature for 20 h and then the saturated NaHCO3 was added. The mixture was extracted with EtOAc and washed with saturated NaCl, dried over Na2SO4 and concentrated. The residue was purified with flash chromatography on silica gel, eluted with a mixture of PE/EA (4/1, v/v) to afford 6a (130 mg, 54%) as a white solid.
  • 4
  • [ 204387-54-2 ]
  • [ 71239-85-5 ]
  • [ 1580457-01-7 ]
YieldReaction ConditionsOperation in experiment
General procedure: Asolution of (2S)-2-[(tert-butoxycarbonyl)amino]-3-(furan-3-yl)propanoicacid (compound 12a, 105 mg, 0.410 mmol) in DMF (5 mL) was added HATU(283 mg, 0.745 mmol) and DIPEA (96 mg, 0.745 mmol). After stirring for 30 mincompound 11 (100 mg, 0.373 mmol) andadditional DIPEA were added. This solution was allowed to stir at roomtemperature for 20 h and then the saturated NaHCO3 was added. Themixture was extracted with EtOAc and washed with saturated NaCl, dried over Na2SO4and concentrated. The residue was purified with flash chromatography on silicagel, eluted with a mixture of PE/EA (4/1, v/v) to afford 13a (105 mg, 85%) as a white solid.
 

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