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Chemical Structure| 115250-39-0 Chemical Structure| 115250-39-0

Structure of 115250-39-0

Chemical Structure| 115250-39-0

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Product Details of [ 115250-39-0 ]

CAS No. :115250-39-0
Formula : C38H45NO7
M.W : 627.77
SMILES Code : OCC(N[C@@H]1[C@H](OCC2=CC=CC=C2)[C@@H](OCC3=CC=CC=C3)[C@H](OCC4=CC=CC=C4)[C@@](O)(COCC5=CC=CC=C5)C1)CO
MDL No. :MFCD11045044

Safety of [ 115250-39-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 115250-39-0 ]

* 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 [ 115250-39-0 ]

[ 115250-39-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 115250-39-0 ]
  • [ 83480-29-9 ]
YieldReaction ConditionsOperation in experiment
82.86% With boron trifluoride diethyl etherate; diisopropylamine; In tetrahydrofuran; at 15 - 30℃; Take 100g of tetrabenzyl voglibose into a 3L three-neck bottle.Add 1200ml of tetrahydrofuran, stir and dissolve, and control the temperature to 15~30 C.104 g of boron trifluoride etherate was added dropwise, and after completion of the reaction,Temperature control 15~30 C, drip diisopropylamine 105g, cool down to 0~5 C,After suction filtration, 450 ml of 90% ethanol was added to the filter cake, and heated to 78-85 C.Stirring for 30~40min, cooling to 0~5C, suction filtration, drying the filter cake under reduced pressure at 40C.35.3 g of a white solid were obtained with a purity of 99.930% and a yield of 82.86%.
With hydrogenchloride; hydrogen;palladium 10% on activated carbon; In tetrahydrofuran; methanol; water; at 20℃; under 2206.72 - 2574.5 Torr; for 3h; To a solution of (lS)-(l (OH), 2,4, 5/1, 3) -2,3, 4-tri-O-benzyl-5-- [ [2-hydroxy-1- (hydroxymethyl) ethyl] amino]-1-C- [benzyloxymethyl]-1, 2,3, 4-cyclohexanetetrol (13.0 g, 20.73 mmol) in methanol : tetrahydrofuran (1: 1,260 mL) were added 10 % palladium- carbon (13 g) and 4% hydrochloric acid solution (20 mL), and the mixture was hydrogenated with shaking for 3 hours at 3.0-3. 5 kg/cm2 at room temperature. The solid was removed by filtration and washed with methanol. The combined filtrate and washings were concentrated. The resulted residue was chromatographed on a column equipped with INDION 890 resin [Ion exchange (India) Ltd. ] with water. The eluent was evaporated under reduced pressure and then treated with ethanol to remove traces of water. Methanol (50 mL) was then added to the residue and stirred at room temperature for 1 hour. The mixture was then filtered and voglibose was obtained as white solid. Yield: 1.5 g HPLC Purity: 97% 'HNMR (D20, 6) : 1. 55 (lH, dd, J: 2.1, 15Hz), 2.10 (lH, dd, J: 2.7, 15Hz), 2.90 (lH, m), 3.40- 3.55 (2H, m), 3.59 (2H, m), 3.64-3. 80 (5H, m), 3.88 (lH, t, J: 9.6Hz).
  • 2
  • [ 115250-39-0 ]
  • 4-benzyl-voglibose [ No CAS ]
  • [ 83480-29-9 ]
YieldReaction ConditionsOperation in experiment
0.7 g; 16 g With formic acid; palladium on activated charcoal; In methanol; water;Inert atmosphere; The synthesis of voglibose from the starting material, d-glucose, to compound 1 referred to the previous reports.9-11 The last step of the adopted method (b) is shown in Scheme 1. After stirring under N2 overnight at room temperature, the solid in the solution of crude compound 1 (44.0 g) was removed by filtration and washed with MeOH/H2O (1:l) several times. The filtrates were combined and concentrated. The residue was separated on a column of Dowex 50W×8 (H+, 2.5 L), washed with H2O and then eluted with 0.5 N ammonium hydroxide. The eluate was concentrated and the crystal of voglibose was obtained in MeOH (16.0 g, 86%). After filtrating the voglibose crystal, the filtrate was concentrated and the residue was separated on a column of silica gel (150 mL) with n-propanol/HOAc/H2O (8:1:l) to give compound 4 (0.7 g, 2.8%) as a pale yellow syrup.
 

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