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Chemical Structure| 111320-77-5 Chemical Structure| 111320-77-5

Structure of 111320-77-5

Chemical Structure| 111320-77-5

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Product Details of [ 111320-77-5 ]

CAS No. :111320-77-5
Formula : C7H16N2O2
M.W : 160.21
SMILES Code : NC[C@H]1OC(C)(C)O[C@@H]1CN

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Application In Synthesis of [ 111320-77-5 ]

* 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 [ 111320-77-5 ]

[ 111320-77-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 111320-77-5 ]
  • [ 349-02-0 ]
  • 4,4'-((((4R,5R)-2,2-dimethyl-1,3-dioxolane-4,5-diyl)bis(methylene))bis(azanediyl))bis(3-nitrobenzamide) [ No CAS ]
YieldReaction ConditionsOperation in experiment
78% With potassium carbonate; In dimethyl sulfoxide; at 70℃; for 1.5h; A mixture of <strong>[349-02-0]4-fluoro-3-nitrobenzamide</strong> (2.233 g, 12.13 mmol), ((4R,5R)-2,2-dimethyl- l,3-dioxolane-4,5-diyl)dimethanamine (0.9713 g, 6.06 mmol), and K2CO3 (1.843 g, 13.34 mmol) in DMSO (20 mL) was stirred at 70 C for 90 min. The reaction was cooled slightly and diluted with 200 mL of water. The resulting orange suspension was stirred vigorously for 60 min, isolated by filtration, the filtered solid was dried in the Buchner funnel for 20 min. The slightly wet solid was transferred to a beaker containing Et20 and the solid was further crushed with a spatula in order to remove excess water from the solid. The resulting solid was isolated by filtration, transferred to a 250 mL RB flask, and dried for 3 days at 56 C in a vacuum oven to give the title product (2.31 g, 4.73 mmol, 78% yield) as a yellow powder. NMR (400 MHz, DMSO-ofe) delta ppm 8.66 (d, 7=2.27 Hz, 2 H) 8.50 (t, 7=5.56 Hz, 2 H) 7.98 - 8.10 (m, 4 H) 7.34 (br. s., 2 H) 7.19 (d, J=9.09 Hz, 2 H) 4.22 (br. s., 2 H) 3.64 - 3.86 (m, 4 H) 1.38 (s, 6 H). LCMS (LCMS Method C): Rt =0.78 min, [M+H]+ = 489.2
78% With potassium carbonate; In dimethyl sulfoxide; at 70℃; for 1.5h; A mixture of <strong>[349-02-0]4-fluoro-3-nitrobenzamide</strong> (2.233 g, 12.13 mmol), ((4R,5R)-2,2-dimethyl- 1,3-dioxolane-4,5-diyl)dimethanamine (0.9713 g, 6.06 mmol), and K2C03 (1.843 g, 13.34 mmol) in DMSO (20 mL) was stirred at 70 C for 90 mm. The reaction was cooled slightly anddiluted with 200 mL of water. The resulting orange suspension was stirred vigorously for 60 mm, isolated by filtration, the filtered solid was dried in the Buchner funnel for 20 mm. The slightly wet solid was transferred to a beaker containing Et20 and the solid was further crushed with a spatula in order to remove excess water from the solid. The resulting solid was isolated by filtration, transferred to a 250 mL RB flask, and dried for 3 days at 56 C in avacuum oven to give the title product (2.31 g, 4.73 mmol, 78% yield) as a yellow powder. 1H NMR (400 MHz, DMSO-o) 3 ppm 8.66 (d, 3=2.27 Hz, 2 H) 8.50 (t, 3=5.56 Hz, 2 H) 7.98 - 8.10 (m, 4 H) 7.34 (br. s., 2 H) 7.19 Cd, J=9.09 Hz, 2 H) 4.22 (br. s., 2 H) 3.64 - 3.86 (m, 4 H) 1.38 Cs, 6 H). LCMS (LCMS Method C): Rt =0.78 mm, [M+H] = 489.2
 

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