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Chemical Structure| 213475-70-8 Chemical Structure| 213475-70-8

Structure of 213475-70-8

Chemical Structure| 213475-70-8

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Product Details of [ 213475-70-8 ]

CAS No. :213475-70-8
Formula : C10H21NO8S2
M.W : 347.41
SMILES Code : O=C(NC(COS(C)(=O)=O)COS(C)(=O)=O)OC(C)(C)C
MDL No. :MFCD18325181

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Application In Synthesis of [ 213475-70-8 ]

* 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 [ 213475-70-8 ]

[ 213475-70-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 125414-41-7 ]
  • [ 124-63-0 ]
  • [ 213475-70-8 ]
YieldReaction ConditionsOperation in experiment
97% With triethylamine; In dichloromethane; at 0 - 20℃; for 2h; To a solution of <strong>[125414-41-7]tert-butyl (1,3-dihydroxypropan-2-yl)carbamate</strong> (21.0 g, 0.1 mol) andTEA (23.0 g, 0.2 mol) in dry CI-bCb (200 mL) was added MsCl (26.0 g, 0.2 mol) at 0 C. Afterthe stirring at room temperature for 2 hrs, the reaction was filtered. The filtrate was concentratedto dryness to give crude 2-((tert-butoxycarbonyl)amino)propane-1,3-diyl dimethanesulfonate(37.0 g, yield: 97%) as a white solid which was used for next step directly without anypurification.
With triethylamine; In dichloromethane; at 5 - 20℃; for 25h; Methanesulfonyl chloride (130 mmol) was added at 5 C to a stirred solution of boc-serinol (40 mol) and triethylamine (25 ml) in dichloromethane (100 ml). The mixture was stirred at 5 C for 5 h and at 20 C for 20 h. Dichloromethane (200 ml) was added and the mixture was washed with an aqueous solution of sodium hydrogen carbonate (50 mM), dried (Na2SO4) and concentrated to dryness under vacuum. Chromatography of the residue on silicagel (1.2 L) eluting with hexane/ethyl acetate (50:50) gave bis-(methanesulfonic acid ester) of boc-serinol.
With triethylamine; In tetrahydrofuran; Referring to Scheme LLL, the amino group in diol 1-29 is protected with Boc2O to provide compound 1-30 which is mesylated (e.g., with MsC1 and TEA) to afford compound 1-31. Compound 1-31 is subjected to a double nucleophilic substitution with pyrazolone 1-9, providing1-32, which is brominated (e.g., with NBS) to afford compound 1-33. Sequential treatment of 1-33 with n-butyl lithium, zinc chloride, and TCPC provides compound 1-34. Intermediate 61 is obtained when 1-34 is reacted with aqueous ammonia.
 

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