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Chemical Structure| 41863-52-9 Chemical Structure| 41863-52-9

Structure of 41863-52-9

Chemical Structure| 41863-52-9

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Product Details of [ 41863-52-9 ]

CAS No. :41863-52-9
Formula : C8H17N3O3
M.W : 203.24
SMILES Code : O=C(OC(C)(C)C)N[C@@H](C)C(NN)=O
MDL No. :MFCD20535463

Safety of [ 41863-52-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Application In Synthesis of [ 41863-52-9 ]

* 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 [ 41863-52-9 ]

[ 41863-52-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 91103-47-8 ]
  • [ 41863-52-9 ]
YieldReaction ConditionsOperation in experiment
93% With hydrazine hydrate; In ethanol; at 20℃; for 5h; To a solution of Intermediate LV (5.35 g, 26.3 mmol) in ethanol (140 mL) wasadded hydrazine hydrate (19.8 mL) and the reaction was stirred at RT for 5 h. Thereaction mixture was concentrated under reduced pressure and the residue was triturated with heptane. The resulting precipitate was collected by filtration and dried in the vacuum oven to afford 5.00 g (93% yield) of the title compound as a white crystalline powder.1H NMR (250 MHz, DMSO): 6 [ppm] 8.96 (5, 1H), 6.81 (d, J = 7.7 Hz, 1H), 4.17 (5,2H), 4.03-3.81 (m, 1H), 1.36 (5, 9H), 1.14 (d, J = 7.1 Hz, 3H).
25% With hydrazine hydrate; In ethanol; Boc-D-alanine methyl ester (2.0 g) was dissolved in ethanol (50 mL)And stirred overnight added hydrazine monohydrate (0.6 mL).After completion of the reaction was partitioned with ethyl acetate and water.The organic layer was washed with a saturated saline solution, and dried over anhydrous sodium sulfate.Concentrated to dryness Insoluble materials were filtered off, the resulting residue was purified by silica gel column chromatography to give the title compound 500mg (25% yield).
With hydrazine; In methanol; at 20℃; for 12h; Hydrazine monohydrate (30 ml) was added to a solution of N-(t-butoxycarbonyl)-D-alanine methyl ester (41.8 g) in methanol (180 ml), and the mixture was stirred at room temperature for 12 hours. The reaction solution was concentrated, and the resulting crude crystal was washed with a mixed solvent of hexane and ethyl acetate (1:1, 300 ml) and then dried to give the titled compound as a colorless powder (32.6 g). 1H NMR (300 MHz, DMDO-d6) delta ppm: 1.14 (d, J = 7.2 Hz, 3H), 1.37 (s, 9H), 3.30-4.09 (m, 3H), 6.70-6.90 (m, 1H), 8.96 (br s, 1H)
With hydrazine; In ethanol; at 20℃; for 16h; To a solution of Boc-D-alanine methyl ester (10 g, 49 mmol) in ethanol (250 mL) was added NH2NH2-H2O (35.6 mL, 735 mmol) and stirred at rt for 16 h. The solvent was removed by evaporation and the residue triturated with hexane to yield a white foamy solid,which was filtered <n="64"/>and dried under vacuum. Yield: 9.8 g. 1HNMR (300 MHz, DMSO-^6) : 8.97 (s, IH)5 6.86-6.84 (m, IH), 4.18 (s, 2H), 3.96-3.86 (m, IH), 1.36 (s, 9H), 1.13 (d, J= 7.14 Hz, 3H). M/Z= 203
11.4 g With hydrazine hydrate; In methanol; at 80℃; for 6h; Step A (R)-tert-butyl (1-hydrazinyl-1-oxopropan-2-yl)carbamate (18a)A solution of N-Boc D-Alanine methyl ester (15 g, 73.891 mmol) and hydrazine hydrate (1 1.08 g, 221.674 mmol) in methanol (200 mL) was heated at 80C for 6h. The reaction mixture was cooled to room temperature and the volatiles were removed under reduced pressure. The crude mass was dissolved in ethyl acetate and washed with water and brine, dried over anhydrous Na2SO4 and evaporated to dryness to afford 18a (11.4 g) which was used as such for next step.
With hydrazine hydrate; In tetrahydrofuran; at 110℃; for 10h;Sealed tube; [0215] To a stuffed solution of compound III (10 g; 41.84 mmol; 1 eq) in THF (30 mL) in a reaction tube was added hydrazine hydrate (6.08 mL; 125.52 mmol; 3 eq). The reaction tube was sealed and heated at 110 C for 10 h. The mixture was concentrated in vacuo to obtain crude title compound (11 g, 100%) as an off white solid. 1H NMR (400 MHz, DMSO-d6) oe 8.98 (brs, 1H), 7.10 (brs, 1H), 6.82 (d, 1H, J= 7Hz), 6.48 (brs, 1H), 4.11 (m, 1H), 1.30 (m, 9H), 1.10 (m, 3H).
8 g With hydrazine hydrate; In ethanol; at 100℃; for 0.5h; Methyl N-(tert-butoxycarbonyl)-D-alaninate (8.00 g, 39.4 mmol) was dissolved in ethanol (10 mL), followed by hydrazine hydrate (20 mL, 410 mmol). The mixture was stirred at 100 SC for 30 min (Caution Use appropriate safety measures). The solvent was removed to obtain tert-butyl [(2R)-1-hydrazinyl-1-oxopropan-2-yl]carbamate (8.00 g, 39.4 mmol).

 

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