Home Cart Sign in  
Chemical Structure| 128726-44-3 Chemical Structure| 128726-44-3

Structure of 128726-44-3

Chemical Structure| 128726-44-3

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 128726-44-3 ]

CAS No. :128726-44-3
Formula : C8H13NO3
M.W : 171.19
SMILES Code : O=C([C@H](CCC1)NC1=O)OCC

Safety of [ 128726-44-3 ]

Application In Synthesis of [ 128726-44-3 ]

* 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 [ 128726-44-3 ]

[ 128726-44-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1117-96-0 ]
  • [ 34622-39-4 ]
  • [ 128726-44-3 ]
  • 2
  • [ 64-17-5 ]
  • [ 34622-39-4 ]
  • [ 128726-44-3 ]
YieldReaction ConditionsOperation in experiment
100% With thionyl chloride; at -5 - 20℃; for 6h; Absolute ethanol (300 mL) was cooled at -5°C then thionyl chloride (14.01 mL, 192.1 mmol) was added keeping the temperature below 0°C, followed by portionwise addiction of (S)-6- oxopiperidine-2-carboxylic acid (25.0 g, 174.6 mmol). The mixture was stirred at room temperature for 6 hours. The solvent was evaporated, then toluene (300 mL) and Et3N (48.7 mL) were added. After 0.5 hour the precipitate was filtered and washed with toluene and Et20. The filtrate was evaporated and the residue treated with Et20. The precipitate was eliminated and the solution was concentrated to give the title compound as yellow oil. Yield (29.9 g, 100percent). H NMR (400 MHz, CDCI3): delta 1 .30 (t, 3H), 1 .75-1 .95 (m, 3H), 2.15-2.25 (m, 1 H), 2.30-2.45 (m, 2H), 4.08 (m, 1 H), 4.24 (q, 2H), 6.43 (br s, 1 H). D2)
100% With thionyl chloride; at 20℃; for 6h; Absolute ethanol (300 mL) was cooled at ?5° C. then thionyl chloride (14.01 mL, 192.1 mmol) was added keeping the temperature below 0° C., followed by portionwise addiction of <strong>[34622-39-4](S)-6-oxopiperidine-2-carboxylic acid</strong> (25.0 g, 174.6 mmol). The mixture was stirred at room temperature for 6 hours. The solvent was evaporated, then toluene (300 mL) and Et3N (48.7 mL) were added. After 0.5 hour the precipitate was filtered and washed with toluene and Et2O. The filtrate was evaporated and the residue treated with Et2O. The precipitate was eliminated and the solution was concentrated to give the title compound as yellow oil. Yield (29.9 g, 100percent). [0132] 1H NMR (400 MHz, CDCl3): delta 1.30 (t, 3H), 1.75-1.95 (m, 3H), 2.15-2.25 (m, 1H), 2.30-2.45 (m, 2H), 4.08 (m, 1H), 4.24 (q, 2H), 6.43 (br s, 1H).
With thionyl chloride; at 20℃; for 16.5h; Step I-1: Ethyl (25)-6-oxo-2-piperidinecarboxylate. To a solution of 6-oxo-L-picolinic acid (5.0Og, 34.9 mmol) in 120 mL EtOH added thionyl chloride (25.5 mL, 349 mmol) in 1 mL aliquots over 30 minutes. After 16 hours of stirring at room temperature, the reaction mixture was concentrated to obtain the desired product containing unidentified impurities as a yellow oil. MS: M+H = 172. The product was used in Step 1-2 without further purification.
6 g With thionyl chloride; at 0 - 20℃;Inert atmosphere; (b) (S)-6-Oxo-piperidine-2-carboxylic acid ethyl ester To a mixture of the product of the previous step (8.4 g, 58.68 mol) in dry ethanol (200 mL) was added thionyl chloride (69.81 g, 586.8 mol) slowly at 0° C. The reaction mixture was stirred at RT overnight and then water was added and the reaction mixture was extracted with EtOAc. The organic layers were washed with sodium bicarbonate and brine, dried over Na2SO4, filtered, and concentrated to provide the title intermediate (6 g). (m/z): [M+H]+ calcd for CsH13NO3 172.09 found 172.1.

 

Historical Records