Home Cart Sign in  
Chemical Structure| 534572-17-3 Chemical Structure| 534572-17-3

Structure of 534572-17-3

Chemical Structure| 534572-17-3

*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 [ 534572-17-3 ]

CAS No. :534572-17-3
Formula : C12H19NO6
M.W : 273.28
SMILES Code : O=C([C@H]1CN(C(OC(C)(C)C)=O)C[C@@H](C(O)=O)C1)O
MDL No. :MFCD29110973
InChI Key :VACTVXMKHNDVTL-OCAPTIKFSA-N
Pubchem ID :18665746

Safety of [ 534572-17-3 ]

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 [ 534572-17-3 ]

* 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 [ 534572-17-3 ]

[ 534572-17-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 4591-55-3 ]
  • [ 24424-99-5 ]
  • [ 534572-17-3 ]
YieldReaction ConditionsOperation in experiment
Reference Example 4(3R,5S)-1-(tert-butoxycarbonyl)piperidine-3,5-dicarboxylic acid Dimethyl pyridine-3,5-dicarboxylate (62.8 g) was dissolved in acetic acid (300 mL), 5% rhodium-carbon (6 g) was added and the mixture was stirred under hydrogen pressurization (5 atm) at 50 C. for 20 hr. The reaction mixture was allowed to cool to room temperature, the rhodium catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The residue was dissolved in methanol (300 mL), and triethylamine (180 mL) and di-tert-butyl bicarbonate (105 g) were successively added under ice-cooling. The reaction mixture was stirred at room temperature for 15 hr, and concentrated under reduced pressure. The residue was dissolved in water, and the mixture was adjusted to pH 3 with 6M hydrochloric acid and extracted with ethyl acetate. The ethyl acetate extraction layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in methanol (300 mL), and 8N aqueous sodium hydroxide solution (161 mL) was added dropwise at room temperature. The reaction mixture was stirred at room temperature for 20 hr, and methanol was evaporated under reduced pressure. The concentrate was diluted with saturated aqueous sodium hydrogen carbonate solution (100 ml) and washed twice with diethyl ether. The basic aqueous layer was acidified (pH 3) with 6M hydrochloric acid. The precipitated powder was collected by filtration, washed with water and air-dried to give the object product (80.5 g) as a powder.1H-NMR (DMSO-d6) delta 1.34-1.43 (9H, m), 1.48 (1H, m), 2.15-2.42 (3H, m), 2.59-2.72 (2H, m), 4.13 (2H, d)
Reference Example 52 (3R,5S)-1-(tert-butoxycarbonyl)piperidine-3,5-dicarboxylic acid [Show Image] Dimethyl pyridine-3,5-dicarboxylate (50 g) was dissolved in acetic acid (300 ml), 5% rhodium carbon (5 g) was added, and the mixture was stirred under pressurized hydrogen atmosphere (5 atm) at 50C for 15 hr. The reaction mixture was allowed to cool to room temperature, the rhodium catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethanol (300 ml) and, under ice-cooling, triethylamine (107 ml) and di-tert-butyl dicarbonate (67 g) were successively added. The reaction mixture was stirred at room temperature for 15 hr, and concentrated under reduced pressure. The residue was dissolved in water, and the mixture was adjusted to pH 3 with 6 M hydrochloric acid. The mixture was extracted with ethyl acetate. The ethyl acetate extract layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in methanol (250 ml), and 8 N aqueous sodium hydroxide solution (128 ml) was added dropwise at room temperature. The reaction mixture was stirred at room temperature for 24 hr, and methanol was evaporated under reduced pressure. The concentrated solution was diluted with saturated aqueous sodium hydrogen carbonate solution (100 ml) and washed twice with diethyl ether. The basic aqueous layer was acidified (pH 3) with 6 M hydrochloric acid. The precipitated powder was collected by filtration, washed with water, and air-dried. The obtained powder (55 g) was dissolved in methanol (200 ml) by heating and the mixture was concentrated under reduced pressure until the amount of methanol became half. Water (50 ml) was added, and the mixture was stood at room temperature overnight. The precipitated white powder was collected by filtration, washed with cold methanol/water=2/1 (200 ml) and air-dried to give the object compound (38 g) as a powder. 1H-NMR (CDCl3) delta 1.47 (9H, s), 1.72 (1H, d), 2.41-2.63 (3H, m), 2.72 (2H, br s), 3.71 (3H, s), 4.38 (2H, d).
  • 2
  • [ 4591-55-3 ]
  • [ 534572-17-3 ]
 

Historical Records

Technical Information

Categories