Home Cart Sign in  
Chemical Structure| 182287-49-6 Chemical Structure| 182287-49-6

Structure of 182287-49-6

Chemical Structure| 182287-49-6

*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 [ 182287-49-6 ]

CAS No. :182287-49-6
Formula : C12H21NO5
M.W : 259.30
SMILES Code : CC(C)(C)OC(=O)NC(C(=O)O)C1CCOCC1
MDL No. :MFCD04114473
InChI Key :MAJWUTNRLZHCBX-UHFFFAOYSA-N
Pubchem ID :22309198

Safety of [ 182287-49-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 182287-49-6 ]

* 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 [ 182287-49-6 ]

[ 182287-49-6 ] Synthesis Path-Downstream   1~11

  • 1
  • [ 477584-90-0 ]
  • [ 182287-49-6 ]
  • 2
  • [ 477585-43-6 ]
  • [ 182287-49-6 ]
  • 3
  • [ 1188366-14-4 ]
  • [ 182287-49-6 ]
YieldReaction ConditionsOperation in experiment
67.8% With lithium hydroxide monohydrate; In tetrahydrofuran; water; at 10 - 35℃; (Step 4) To a solution of methyl 2-((tert-butoxycarbonyl)amino)-2-(tetrahydro-2H-pyran-4-yl)acetate (4.77 g, 17.45 mmol) in a mixed solvent of THF (10 mL) and water (4 mL) was added lithium hydroxide monohydrate (1.099 g, 26.18 mmol), and the mixture was stirred overnight at room temperature. THF was evaporated under reduced pressure, 1N hydrochloric acid was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure to give 2-((tert-butoxycarbonyl)amino)-2-(tetrahydro-2H-pyran-4-yl)acetic acid (3.07 g, 11.84 mmol, 67.8%) as a white solid. 1H NMR(300 MHz, CDCl3):δ1.45(9H,s), 1.48-1.68(4H,m), 1.92-2.21(1H,m),3.27-3.50(2H,m),4.02(2H,d,J=11.0 Hz),4.29(1H,brs),5.14(1H,d,J=8.3 Hz). (COOH group hydrogen was not observed.)
  • 4
  • [ 182287-49-6 ]
  • (3S)-1-(2-(methylamino)-2-(tetrahydro-2H-pyran-4-yl)ethyl)pyrrolidin-3-ol [ No CAS ]
  • 5
  • [ 182287-49-6 ]
  • [ 100243-39-8 ]
  • [ 1455472-20-4 ]
  • 6
  • [ 29943-42-8 ]
  • [ 182287-49-6 ]
  • 7
  • [ 182287-49-6 ]
  • [ 52756-36-2 ]
  • tert-butyl (2-((4-(tert-butyl)-3-chlorophenyl)amino)-2-oxo-1-(tetrahydro-2H-pyran-4-yl)ethyl)carbamate [ No CAS ]
YieldReaction ConditionsOperation in experiment
88% With dmap; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine; In water; ethyl acetate; at 10 - 60℃; (Step 8) To a solution of 2-((tert-butoxycarbonyl)amino)-2-(tetrahydro-2H-pyran-4-yl)acetic acid (1.55 g, 5.98 mmol), 4-(tert-butyl)-3-chloroaniline (1.098 g, 5.98 mol), DMAP (0.803 g, 6.58 mmol) and DIEA (5.22 mL, 29.89 mmol) in ethyl acetate (20 mL) was added T3P (5.27 mL, 8.97 mmol) at room temperature. The reaction mixture was stirred overnight at 60C, water and ethyl acetate were added thereto, and the organic layer was separated. The organic layer was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure to give tert-butyl (2-((4-(tert-butyl)-3-chlorophenyl)amino)-2-oxo-1-(tetrahydro-2H-pyran-4-yl)ethyl)carbamate (2.23 g, 5.25 mmol, 88%) as a white solid. 1H NMR(300 MHz,CDCl3):δ1.41-1.51(19H,m), 1.59-1.72(2H,m), 2.08-2.25(1H,m),3.39(2H,t,J=11.7 Hz),3.90-4.07(3H,m),5.07(1H,d,J=7.9 Hz),7.29-7.41(3H,m),7.56-7.63(1H,m), 7.95(1H,brs).
  • 8
  • [ 182287-49-6 ]
  • tert-butyl ((1R)-2-((4-(tert-butyl)-3-chlorophenyl)amino)-2-oxo-1-(tetrahydro-2H-pyran-4-yl)ethyl)carbamate [ No CAS ]
  • 9
  • [ 182287-49-6 ]
  • (2R)-2-amino-N-(4-(tert-butyl)-3-chlorophenyl)-2-(tetrahydro-2H-pyran-4-yl)acetamide hydrochloride [ No CAS ]
  • 10
  • [ 182287-49-6 ]
  • N-((1R)-2-((4-tert-butyl-3-chlorophenyl)amino)-2-oxo-1-(tetrahydro-2H-pyran-4-yl)ethyl)-3,3,3-trifluoropropanamide [ No CAS ]
  • 11
  • [ 182287-49-6 ]
  • N-((1R)-2-((4-tert-butyl-3-chlorophenyl)amino)-2-oxo-1-(tetrahydro-2H-pyran-4-yl)ethyl)-3,3,3-trifluoro-2-hydroxypropanamide [ No CAS ]
 

Historical Records

Technical Information

Categories