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Chemical Structure| 1449330-32-8 Chemical Structure| 1449330-32-8

Structure of 1449330-32-8

Chemical Structure| 1449330-32-8

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Product Details of [ 1449330-32-8 ]

CAS No. :1449330-32-8
Formula : C15H19ClN2O4
M.W : 326.78
SMILES Code : O=C(N1CC(C(OC)=O)(C2=NC=C(Cl)C=C2)C1)OC(C)(C)C
MDL No. :MFCD28053495

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Application In Synthesis of [ 1449330-32-8 ]

* 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 [ 1449330-32-8 ]

[ 1449330-32-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1480-65-5 ]
  • [ 610791-05-4 ]
  • [ 1449330-32-8 ]
YieldReaction ConditionsOperation in experiment
19% With potassium hexamethylsilazane; In toluene; at 0 - 20℃; for 3.5h; To a solution of 5-chloro-2-fluoropyridine (0.5 g, 3.8 mmol, Eq: 1.00) and 1-tert-butyl 3- methyl azetidine-l,3-dicarboxylate (818 mg, 3.8 mmol, Eq: 1.00) in toluene (5 ml) was added dropwise at 0°C for 15 min a 0.5 M solution of KHMDS (7.6 ml, 3.8 mmol, Eq: 1.00) in toluene. The colorless solution turned into yellow-orange. After stirring at 0°C for 45 min, the reaction mixture was allowed to warm to 20°C and stirred for 2.5 h. A saturated aqueous NH4C1 solution (50 ml) was added and the aqueous phase was extracted with AcOEt (2 x 75 ml). The combined organic layers were washed with brine, dried over Na2S04, filtered and concentrated under reduced pressure. The crude material was purified by flash chromatography (silica gel, 12 g, 10percent to 60percent AcOEt in heptane) to yield a colorless gum (0.234 g; 19percent). m/z = 327.2 [M+H]+.
19% With potassium hexamethylsilazane; In toluene; at 0 - 20℃; for 3.5h; To a solution of 5-chloro-2-fluoropyridine (0.5 g, 3.8 mmol, Eq: 1.00) and <strong>[610791-05-4]1-tert-butyl 3-methyl azetidine-1,3-dicarboxylate</strong> (818 mg, 3.8 mmol, Eq: 1.00) in toluene (5 ml) was added dropwise at 0° C. for 15 min a 0.5 M solution of KHMDS (7.6 ml, 3.8 mmol, Eq: 1.00) in toluene. The colorless solution turned into yellow-orange. After stirring at 0° C. for 45 min, the reaction mixture was allowed to warm to 20° C. and stirred for 2.5 h. A saturated aqueous NH4Cl solution (50 ml) was added and the aqueous phase was extracted with AcOEt (2×75 ml). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The crude material was purified by flash chromatography (silica gel, 12 g, 10percent to 60percent AcOEt in heptane) to yield a colorless gum (0.234 g; 19percent). m/z=327.2 [M+H]+.
 

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