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Chemical Structure| 274692-06-7

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Product Details of [ 274692-06-7 ]

CAS No. :274692-06-7
Formula : C11H21NO5S
M.W : 279.35
SMILES Code : O=C(N1C[C@@H](COS(=O)(C)=O)CC1)OC(C)(C)C
MDL No. :MFCD14635772

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Application In Synthesis of [ 274692-06-7 ]

* 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 [ 274692-06-7 ]

[ 274692-06-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 124-63-0 ]
  • [ 199174-24-8 ]
  • [ 274692-06-7 ]
YieldReaction ConditionsOperation in experiment
90% With triethylamine; In dichloromethane; at 0 - 20℃; for 4h; To a solution of <strong>[199174-24-8]tert-butyl (S)-3-(hydroxymethyl)pyrrolidine-1-carboxylate</strong> (2.0 g, 9.9 mmol) and triethylamine (2.8 mL, 19.8 mmol) in methylene chloride (50.0 mL) at 0C was dropwise added methanesulfonyl chloride (0.85 mL, 10.9 mmol). The reaction mixture was stirred at ambient temperature for 4 hours and then washed sequentially with 0.1 N hydrogen chloride and brine. The organic layer was dried over Na2S04 filtered, and concentrated in vacuo to yield 2.5 g (90 %) of the title product as an oil.
90% With triethylamine; In dichloromethane; at 0 - 20℃; for 4h; [0563] To a solution of <strong>[199174-24-8]tert-butyl (S)-3-(hydroxymethyl)pyrrolidine-1-carboxylate</strong> (2.0 g, 9.9 mmol) and triethylamine (2.8 mL, 19.8 mmol) in methylene chloride (50.0 mL) at 0C was dropwise added methanesulfonyl chloride (0.85 mL, 10.9 mmol). The reaction mixture was stirred at ambient temperature for 4 hours and then washed sequentially with 0.1 N hydrogen chloride and brine. The organic layer was dried over Na2SO4 filtered, and concentrated in vacuo to yield 2.5 g (90 %) of the title product as an oil. [M+1]+ 280.
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0℃; for 2h;Product distribution / selectivity; a) 1,1-dimethylethyl 3-[(methylsulfonyl)oxy]methyl}-l-pyrrolidinecarboxylateA solution of 1,1-dimethylethyl 3-(hydroxymethyl)-l-pyrrolidinecarboxylate (3.051 mmol) and DIPEA (4.576 mmol) in CH2C12 (10 mL) was cooled to 0 C, treated with MsCl (3.051 mmol), and stirred at 0 C for 2 h. The reaction mixture was then diluted with water and CH2C12 (50 mL). After separating the layers, the aqueous layer was further extracted with CH2C12 (2 x 20 mL). The combined organic layers were dried over Na2S04 and concentrated in vacuo to provide the crude title compound (0.838 g) as an amber oil. LCMS (ES+) m/z 280 [M+H]+.
  • 2
  • [ 274692-06-7 ]
  • [ 274692-08-9 ]
 

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