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Chemical Structure| 135080-10-3 Chemical Structure| 135080-10-3

Structure of 135080-10-3

Chemical Structure| 135080-10-3

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Product Details of [ 135080-10-3 ]

CAS No. :135080-10-3
Formula : C6H7NO4S2
M.W : 221.25
SMILES Code : O=C(C1=CC=C(S(=O)(NC)=O)S1)O

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Application In Synthesis of [ 135080-10-3 ]

* 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 [ 135080-10-3 ]

[ 135080-10-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 114365-04-7 ]
  • [ 135080-10-3 ]
  • 5-(N-methylsulfamoyl)-N-(4-(pyrrolidin-1-yl)benzyl)thiophene-2-carboxamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
9% With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 0 - 20℃; for 16h; To a stirred solution of a3 (200 mg, 0.9040 mmol) in DMF (10 mL), was added HATU (443 mg, 1.1651 mmol) and DIPEA (323 mg, 2.499 mmol) followed by corresponding amine (244 mg, 1.3843 mmol) at 0 C. The reaction mixture was stirred at room temperature for 16 h. The reaction mixture was quenched with water (10 mL) and extracted with EtOAc (2 X 50 mL). The combined organic layers were dried over NaiSCE and concentrated under reduced pressure. The crude material was purified by flash column chromatography using EtOAc in heptane = 0% to 35% to 90% as an eluent to afford 30 (27.6 mg, 0.0802 mmol, 9%). LCMS: 380.2 (M+H), Rt = 3.389 min, ColummX-Bridge BEH C- 18(3.0X50mm,2.5pm); Mobile Phase: A:2.5mM Ammonium Bicarbonate, B:ACN; (Gradient) T/B%:0.01/10, 3/90, 5/90, 5.5/10, 6/10; Flow rate:0.8ml/min. HPLC: Rt = 9.58 min, 97.12%; Mobile Phase A : 5mM Ammonium Bi Carbonate; Mobile Phase B : Acetonitrile; Program :T/B% :0.01/20, 12/90, 16/90; Flow : l.OmL/min; Diluent :: WATER: ACN. 'll NMR (400 MHz, DMSO-d6) 9.16 (t, 1H), 7.79 (d, 2H), 7.56 (d, 1H), 7.11 (d, 2H), 6.49 (d, 2H), 4.32 (d, 2H), 3.14 (t, 4H), 1.93 (t, 4H), 3 H Merged in solvent peak.
9% With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 0 - 20℃; for 16h; To a stirred solution of a3 (200 mg, 0.9040 mmol) in DMF (10 mL), was added HATU (443 mg, 1.1651 mmol) and DIPEA (323 mg, 2.499 mmol) followed by corresponding amine (244 mg, 1.3843 mmol) at 0 C. The reaction mixture was stirred at room temperature for 16 h. The reaction mixture was quenched with water (10 mL) and extracted with EtOAc (2 X 50 mL). The combined organic layers were dried over NaiSCE and concentrated under reduced pressure. The crude material was purified by flash column chromatography using EtOAc in heptane = 0% to 35% to 90% as an eluent to afford 30 (27.6 mg, 0.0802 mmol, 9%). LCMS: 380.2 (M+H), Rt = 3.389 min, ColummX-Bridge BEH C- 18(3.0X50mm,2.5pm); Mobile Phase: A:2.5mM Ammonium Bicarbonate, B:ACN; (Gradient) T/B%:0.01/10, 3/90, 5/90, 5.5/10, 6/10; Flow rate:0.8ml/min. HPLC: Rt = 9.58 min, 97.12%; Mobile Phase A : 5mM Ammonium Bi Carbonate; Mobile Phase B : Acetonitrile; Program :T/B% :0.01/20, 12/90, 16/90; Flow : l.OmL/min; Diluent :: WATER: ACN. 'll NMR (400 MHz, DMSO-d6) 9.16 (t, 1H), 7.79 (d, 2H), 7.56 (d, 1H), 7.11 (d, 2H), 6.49 (d, 2H), 4.32 (d, 2H), 3.14 (t, 4H), 1.93 (t, 4H), 3 H Merged in solvent peak.
 

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