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Chemical Structure| 154743-05-2 Chemical Structure| 154743-05-2

Structure of 154743-05-2

Chemical Structure| 154743-05-2

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Product Details of [ 154743-05-2 ]

CAS No. :154743-05-2
Formula : C3H10N2O2S
M.W : 138.19
SMILES Code : NS(=O)(N(CC)C)=O
MDL No. :MFCD11623179

Safety of [ 154743-05-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 154743-05-2 ]

* 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 [ 154743-05-2 ]

[ 154743-05-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 154743-05-2 ]
  • [ 159622-10-3 ]
  • [ 1028251-26-4 ]
YieldReaction ConditionsOperation in experiment
With 1,1'-carbonyldiimidazole; lithium hexamethyldisilazane; In tetrahydrofuran; hexane; at 20℃; for 3.75h;Heating / reflux; Step 1 of Example 19 To a solution of (1R, 2S) l-tert-butoxycarbonylamino-2-vinyl- cyclopropanecarboxylic acid (217 mg, 1.194 mmol) in THF (5 mL), CDI (290 mg, 1. 791 mmol) was added and the reaction mixture was heated under reflux for 45 min. In another round-bottomed flask, LiHMDS (1.0 M solution in hexanes, 2.4 mL, 2.4 mmol) was added to a solution of N-ethylmethylsulfamide (330 mg, 2.388 mmol) in THF (5 mL) and the reaction mixture was stirred at rt for lh. Two reaction mixtures were added together and stirred at rt for 2h. Water was added to quench the reaction and the reaction solution was extracted with EtOAc. The oraganic layer was separated and dried over MgS04. Evaporation of solvent gave crude product which was purified by Prep. HPLC to afford desired N-acylsulfamide. N-acylsulfamide was then dissolved in 4N HC1 solution in dioxane (2mL) and stirred at rt for 4h. Evaporation of solution give brownish oil as HCl salt. (112mg, 33percent yield). 1H NMR (400Mz, CD30D) delta 1. 16 (t, J=7. 21 Hz, 3 H), 1.68 (dd, J=10. 03,7. 83 Hz, 1 H), 2.15 (m, 1 H), 2.37 (m, 1 H), 2.89 (s, 3 H), 3.30 (m, 2 H), 5.31 (d, J=10. 27 Hz, 1 H), 5.42 (d, J=17. 12 Hz, 3 H), 5.68 (m, 1 H). LC-MS (retention time: 0.883 min. ), MS m/z 270 (M+Na+).
13. Preparation of P1-P1' Sulfamide Derivative; To a solution of (1R,2S) 1-tert-butoxycarbonylamino-2-vinyl-cyclopropanecarboxylic acid (217 mg, 1.194 mmol) in THF (5 mL), was added CDI (290 mg, 1.791 mmol) and the reaction mixture was heated to reflux for 45 minutes. In another round-bottomed flask, LiHMDS (1.0M solution in hexanes, 2.4 mL, 2.4 mmol) was added to a solution of N-ethylmethylsulfamide (330 mg, 2.388 mmol) in THF (5 mL) and the reaction mixture was stirred at room temperature for 1 hour. The two reaction mixtures were combined and stirred at room temperature for 2 hours. Water was added to quench the reaction and the reaction solution was extracted with ethyl acetate. The organic layer was separated and dried over MgSO4. Filtration and concentration gave crude product which was purified by preparative HPLC to provide the desired N-Boc protected N-acylsulfamide. The Boc protecting group was then removed as the compound was dissolved in 4N HCl solution in dioxane (2 mL) and stirred at room temperature for 4 hours. Concentration provided a brownish oil as the HCl salt. (112 mg, 33percent yield). 1H NMR (400Mz, CD3OD) delta 1.16 (t, J=7.21 Hz, 3H), 1.68 (dd, J=10.03, 7.83 Hz, 1H), 2.15 (m, 1H), 2.37 (m, 1H), 2.89 (s, 3H), 3.30 (m, 2H), 5.31 (d, J=10.27 Hz, 1H), 5.42 (d, J=17.12 Hz, 3H), 5.68 (m, 1H). LC-MS (retention time: 0.883 minutes.), MS m/z 270 (M+Na+).
 

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