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Chemical Structure| 159700-60-4 Chemical Structure| 159700-60-4

Structure of 159700-60-4

Chemical Structure| 159700-60-4

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Product Details of [ 159700-60-4 ]

CAS No. :159700-60-4
Formula : C11H19NO4
M.W : 229.27
SMILES Code : O=C([C@]1(NC(OC(C)(C)C)=O)[C@H](CC)C1)O

Safety of [ 159700-60-4 ]

Application In Synthesis of [ 159700-60-4 ]

* 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 [ 159700-60-4 ]

[ 159700-60-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 159622-10-3 ]
  • [ 159700-60-4 ]
YieldReaction ConditionsOperation in experiment
49% With 10 wt% Pd(OH)2 on carbon; hydrogen; In tert-butyl methyl ether; under 760.051 Torr; for 3h; 2 was prepared by a modification of the procedure published in the literature (J. Org. Chem., 2005, 70, 5869). 1 (1.004 g, 4.40 mmol) was dissolved in TI3ME (25 ml) and hydrogenated (1 atm hydrogen gas) over 20percent Pd(OH)2/C (150 mgs)for 3 hours. The suspension was then filtered on celite and thecrude concentrated under reduced pressure. The crude is crystallized from water-ethanol. The crude is taken in 100 ml water and heated to 70° C. and ethanol is added drop wise until the solution becomes cleat The solution is lefi overnight to cool and the solids are filtered to get the pure product 2 (494 mgs, 2.155 mmol, 49percent yield). The pure product is dried under vacuum.
42% With hydrogen;palladium hydroxide on carbon; In tert-butyl methyl ether; at 20℃; under 760.051 Torr; for 5h;Product distribution / selectivity; Compound 23; (1R,2R )-1-(tert-butoxycarbonylamino)-2-ethy]cyclopropanecarboxylic acid; (1R,2S)-1-(tert-butoxycarbonyl)-2-vinylcyclopropanecarboxyhc acid (10 0 g, 44 0 mmol, prepared as described in WO2005037214) was dissolved m MTBE (250 mL) and hydrogenated (1 atm H2) over Pd(OH)2/C (1 24 g, 8.80 mmol) for 5 h at rt The reaction was then stopped, filtered and concentrated down to 30 mL, followed by addition of 300 mL hexanes while stirring vigorously After 60 mm, the fine white precipitate was filtered, yielding the titled compound as a fine off-white powder (4 2 g, 42 percent yield) 1H-NMR (400 MHz, d6-DMSO) delta 12 2 (s, 1 H), 7 41 (s, 1 H), 1.29 - 1 54 (m, 3 H), 1 36 (s, 9 H), 1 18 - 1 21 (m, 1 H), 0 96 - 0 98 (m, 1 H), 0 90 (t, 3 H); (1R,2R)-1-(tert-butoxycarbonylamino)-2-ethylcyclopropanecarboxylic acid; (li,25)-1-(tert-butoxycarbonyl)-2-vinyIcyclopropanecarboxylic acid (10.0 g, 44.0 mmol, prepared as described in WO2005037214) was dissolved in MTBE (250 mL) and hydrogenated (1 atm H2) over Pd(OH)2/C (1.24 g, 8.80 mmol) for 5 h at rt. The reaction was then stopped, filtered and concentrated down to 30 mL, followed by addition of 300 mL hexanes while stirring vigorously. After 60 min, the fine white precipitate was filtered, yielding the titled compound as a fine off-white powder (4.2 g, 42 percent yield). 1H-NMR (400 MHz, d6-DMSO) delta 12.2 (s, 1 H), 7.41 (s, 1 H), 1.29 - 1.54 (m, 3 H), 1.36 (s, 9 H), 1.18 - 1.21 (m, 1 H), 0.96 - 0.98 (m, 1 H), 0.90 (t, 3 H).
  • 2
  • [ 154350-29-5 ]
  • [ 159700-60-4 ]
  • [ 923591-34-8 ]
YieldReaction ConditionsOperation in experiment
73% Compound 73; Compound 73 was prepared as described herein; Step 1: Synthesis of tert-butyl (1R,2S )-1-(cyclopropylsulfonylcarbamoyl)-2- ethylcyclopropylcarbamate; (1R,2S)-1-(tert-butoxycarbonyl)-2-ethylcyclopropanecarboxylic acid (0.5 g, 2.18 mmol) was dissolved in THF (20 mL), followed by addition of CDI (390 mg, 2.41 mmol) in one portion at rt. The reaction was stirred in a 60 C sandbath for 4 h, cooled to it, and <strong>[154350-29-5]cyclopropanesulfonamide</strong> (292 mg, 2.41 mmol) and DBU (366 mg, 2.41 mmol) were added. The reaction was stirred at rt for overnight. The reaction was then diluted with <n="153"/>EtOAc (30 mL) and washed with 1 N HCl (2 x 15 raL), water (10 mL), brine (10 mL), and dried (Na2SO4), giving tert-butyl (lJ?,2JR)-1-(cyclopropylsulfonylcarbamoyl)-2- ethylcyclopropylcarbamate(0.53 g, 73% yield) as a white solid after removal of solvent. This crude product was directly used for the next without further purification.
 

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