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Chemical Structure| 17042-39-6 Chemical Structure| 17042-39-6

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Chemical Structure| 17042-39-6

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Product Details of [ 17042-39-6 ]

CAS No. :17042-39-6
Formula : C20H23NO12
M.W : 469.40
SMILES Code : O=[N+](C1=CC=C(O[C@@H]2[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H](COC(C)=O)O2)C=C1)[O-]
MDL No. :MFCD00023841

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Application In Synthesis of [ 17042-39-6 ]

* 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 [ 17042-39-6 ]

[ 17042-39-6 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 108-24-7 ]
  • [ 7493-95-0 ]
  • [ 17042-39-6 ]
YieldReaction ConditionsOperation in experiment
100% With pyridine; dmap; at 20.0℃; for 4.0h;Inert atmosphere; To a solution of p-nitrophenyl galactopyranoside 4b (5.0 g, 16.6 mmol) in anhydrous pyridine (50 mL) was added acetic anhydride (25 mL) and 4-dimethylaminopyridine (DMAP) (50 mg), and the reaction mixture was stirred at room temperature for 4 h. The progress of reaction was checked by TLC (CHCl3:MeOH; 9:1, v/v). After completion of reaction, the solvent was removed under vacuum. The residue was dissolved in chloroform (200 mL) and washed with cold aq. HCl (2%), water and brine, and dried over sodium sulfate, concentrated under reduced pressure to afford the intermediate 2,3,4,5-tetracetyl-p-nitrophenyl-alpha-D-galactopyranoside (7.98 g. 100%) as an off-white solid. The peracetylated nitro compound (7.98 g,17.0 mmol) was dissolved in a mixture of warm methanol(200 mL) and ethyl acetate (150 mL). The solution was treatedwith 10% palladium on carbon (2.2 g) in ethyl acetate (10 mL) in small portions, followed by ammonium formate (23 g, 0.36 mol) and the reaction mixture was stirred at room temperature for 30 min. The progress of reaction was checked by TLC (CHCl3:MeOH; 9.5:0.5, v/v). The reaction mixture was filtered through celite bed immediately after completion of reaction and the bed was washed with a mixture of ethyl acetate (75 mL) and methanol (25 mL). The filtrate and the washings were combined and concentrated under vacuum. The residue was again dissolved in ethyl acetate (300 mL) and washed with water (3100 mL) and brine, dried over sodium sulfate and concentrated under vacuum. The compound 6b was desiccated overnight and used in next step without purification (6.7 g;89.7%) as off white solid. Mp 131-132 C; [alpha]D25 + 176.4(c 1.0, CHCl3); IR (KBr): 3325, 2925, 2854, 1749, 1660, 1511, 1373, 1231,1070 cm-1; 1H NMR (400 MHZ, CDCl3): d 1.98 (s, 3H), 2.02 (s, 3H),2.08 (s, 3H), 2.16 (s, 3H), 4.12 (m, 2H), 4.40 (t, 1H, J = 6.85 Hz),5.25 (dd, 1H, J1 = 3.79 Hz, J2 = 2 = 3.59 Hz), 5.53-5.56 (m, 2H), 5.59(d, 1H, J = 3.83 Hz), 6.61 (d, 2H, J = 8.91 Hz), 6.86 (d, 2H, J = 8.63); 13C NMR (100 MHz, CDCl3): d 20.55, 20.59, 20.68, 61.55, 66.87,67.55, 67.92, 67.98, 76.68, 76.99, 77.32, 99.99, 115.92, 118.33,142.18, 149.16, 169.93, 170.12, 170.25, 170.30; HRMS (ESI) Calcd.for C20H25NO10 (M + H+) 440.1551, found: 440.1520.
100% With pyridine; dmap; at 20.0℃; for 4.0h;Inert atmosphere; To a solution of p-nitrophenyl galactopyranoside 4b (5.0 g,16.6 mmol) in anhydrous pyridine (50 mL) was added aceticanhydride (25 mL) and 4-dimethylaminopyridine (DMAP)(50 mg), and the reaction mixture was stirred at roomtemperature for 4 h. The progress of reaction was checked byTLC (CHCl3:MeOH; 9:1, v/v). After completion of reaction, thesolvent was removed under vacuum. The residue was dissolvedin chloroform (200 mL) and washed with cold aq. HCl (2%),water and brine, and dried over sodium sulfate, concentratedunder reduced pressure to afford the intermediate 2,3,4,5-tetracetyl-p-nitrophenyl-a-D-galactopyranoside (7.98 g. 100%) asan off-white solid. The peracetylated nitro compound (7.98 g,17.0 mmol) was dissolved in a mixture of warm methanol(200 mL) and ethyl acetate (150 mL). The solution was treatedwith 10% palladium on carbon (2.2 g) in ethyl acetate (10 mL) insmall portions, followed by ammonium formate (23 g, 0.36 mol)and the reaction mixture was stirred at room temperature for30 min. The progress of reaction was checked by TLC (CHCl3:MeOH; 9.5:0.5, v/v). The reaction mixture wasfiltered throughcelite bed immediately after completion of reaction and the bedwas washed with a mixture of ethyl acetate (75 mL) andmethanol (25 mL). Thefiltrate and the washings were combinedand concentrated under vacuum. The residue was againdissolved in ethyl acetate (300 mL) and washed with water(3100 mL) and brine, dried over sodium sulfate and concentratedunder vacuum. The compound 6b was desiccatedovernight and used in next step without purification (6.7 g;89.7%) as off white solid. Mp 131-132 C; [a]D25 + 176.4(c 1.0,CHCl3); IR (KBr): 3325, 2925, 2854, 1749, 1660, 1511, 1373, 1231,1070 cm1; 1H NMR (400 MHZ, CDCl3): d 1.98 (s, 3H), 2.02 (s, 3H),2.08 (s, 3H), 2.16 (s, 3H), 4.12 (m, 2H), 4.40 (t, 1H, J = 6.85 Hz),5.25 (dd, 1H, J1 = 3.79 Hz, J2 = 2 = 3.59 Hz), 5.53-5.56 (m, 2H), 5.59(d, 1H, J = 3.83 Hz), 6.61 (d, 2H, J = 8.91 Hz), 6.86 (d, 2H, J = 8.63);13C NMR (100 MHZ, CDCl3): d 20.55, 20.59, 20.68, 61.55, 66.87,67.55, 67.92, 67.98, 76.68, 76.99, 77.32, 99.99, 115.92, 118.33,142.18, 149.16, 169.93, 170.12, 170.25, 170.30; HRMS (ESI) Calcd.for C20H25NO10 (M + H+) 440.1551, found: 440.1520.
 

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