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Chemical Structure| 209328-53-0 Chemical Structure| 209328-53-0

Structure of 209328-53-0

Chemical Structure| 209328-53-0

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Product Details of [ 209328-53-0 ]

CAS No. :209328-53-0
Formula : C16H23NO5S
M.W : 341.42
SMILES Code : O=C(N1[C@H](COS(=O)(C2=CC=C(C)C=C2)=O)CC1)OC(C)(C)C
MDL No. :MFCD27976345

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Application In Synthesis of [ 209328-53-0 ]

* 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 [ 209328-53-0 ]

[ 209328-53-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 98-59-9 ]
  • [ 161511-85-9 ]
  • [ 209328-53-0 ]
YieldReaction ConditionsOperation in experiment
96% With pyridine; In dichloromethane; at 20℃;Cooling with ice; To a solution of [l-(?ert-butoxycarbonyl)-2(lSr)-azetidinyl]methanol (3.74 g, 20 mmol) and pyridine (24 g, 300 mmol, 15 equiv.) in CH2Cl2 (20 mL) was added p- toluenesulfonyl chloride (5.72 g, 30 mmol, 1.5 equiv.) with ice cooling under N2. The solution was stirred overnight at room temperature and diluted with water. After phase separation, the aqueous layer was extracted with EtOAc (3 x 100 mL). The combined organic layers were washed with saturated aqueous NH4Cl solution and brine, dried over Na2SO4, and concentrated. The residue was loaded onto a silica gel column, which was eluted with EtO Ac/petroleum ether 1:10 to give the tosylate (6.5 g, 96%) as a colorless oil. 1H NMR (CDCl3, 500 MHz) δ 7.82 (d, 2H, J = 8.2 Hz), 7.37 (d, IH, J = 8.0 Hz), 4.35 (br s, IH), 4.26 (br s, IH), 4.15 (dd, IH, J = 10.2, 2.8 Hz), 3.84-3.77 (m, 2H), 2.46 (s, 3H), 2.30-2.23 (m, IH), 2.17 (br s, IH), 1.39 (s, 9H). LC-MS (ESI) m/z 364 (M+Na+).
In pyridine; 10b. (S)-1-t-butyloxycarbonyl-2-toluensulfonyloxymethylazetidine A solution of <strong>[161511-85-9](2S)-1-t-butyloxycarbonyl-2-azetidinemethanol</strong> (22.6 g, 0.121 mol) in 40 mL of pyridine was treated with p-toluenesulfonyl chloride (27.6 g, 0.145 mol). The resulting mixture was stirred at room temperature for 16 hours, diluted with CH2 Cl2 and washed sequentially with 1 N aqueous HCl, H2 O, saturated aqueous K2 CO3, and brine. The organic phase was dried (Na2 SO4) and concentrated. Purification by chromatography (silica gel; Hexane/EtOAc, 80:20) afforded 32.8 g of a white solid which was recrystallized from CH2 Cl2 /hexane to afford the title compound as thin white needles: mp 59-60 C.; 1 H NMR (CDCl3, 300 MHz) δ 1.37 (s, 9H), 2.15-3.28 (m, 2H), 2.44 (s, 3H), 3.74-3.81 (m, 2H), 4.13 (dd, J=3.1, 10.2 Hz, 1 H), 4.23-4.34 (m, 2H), 7.35 (d, J=8.1 Hz, 2H), 7.80 (d, J=8.2 Hz, 2H); MS (CI/NH3) m/z: 242 (M+H)+.
 

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