Home Cart Sign in  
Chemical Structure| 1138820-45-7 Chemical Structure| 1138820-45-7

Structure of 1138820-45-7

Chemical Structure| 1138820-45-7

*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 [ 1138820-45-7 ]

CAS No. :1138820-45-7
Formula : C11H18F3NO5S
M.W : 333.33
SMILES Code : O=C(N1CCC(OS(=O)(C(F)(F)F)=O)CC1)OC(C)(C)C

Safety of [ 1138820-45-7 ]

Application In Synthesis of [ 1138820-45-7 ]

* 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 [ 1138820-45-7 ]

[ 1138820-45-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1138820-45-7 ]
  • [ 4983-28-2 ]
  • [ 1314391-51-9 ]
YieldReaction ConditionsOperation in experiment
31.7% With potassium carbonate; In dimethyl sulfoxide; at 110℃; for 16h; A suspension of tert-butyl 4-(((trifluoromethylsulfonyl)oxy)piperidine-1-carboxylate (6.2 g, 21.1 mmol), <strong>[4983-28-2]2-chloropyrimidin-5-ol</strong> (2.5 g, 19.2 mmol) and potassium carbonate ( 13.3 g, 96 mmol) in dimethylsulfoxide (100 mL) was stirred at llOoC for 16 hours. The reaction mixture was cooled to room temperature and dimethylsulfoxide was distilled off under reduced pressure. The residue was then treated with water (50 mL) and precipitate was formed, filtered off and purified by column chromatography eluting with hexanes: ethyl acetate mixture (3:2) by volume to afford the title compound (2.0 g, 31.7 %) as a white crystalline powder:
31.7% With potassium carbonate; In dimethyl sulfoxide; at 110℃; for 16h; [0545] A suspension of tert-butyl 4-(((trifluoromethylsulfonyl)oxy)piperidine-1-carboxylate (6.2 g, 21.1 mmol), <strong>[4983-28-2]2-chloropyrimidin-5-ol</strong> (2.5 g, 19.2 mmol) and potassium carbonate (13.3 g, 96 mmol) in dimethylsulfoxide (100 mL) was stirred at 110 for 16 hours. The reaction mixture was cooled to room temperature and dimethylsulfoxide was distilled off under reduced pressure. The residue was then treated with water (50 mL) and precipitate was formed, filtered off and purified by column chromatography eluting with hexanes: ethyl acetate mixture (3:2) by volume to afford the title compound (2.0 g, 31.7 %) as a white crystalline powder: 1H NMR (400 MHz, DMSO-d6) delta 8.53 (s, 2H), 4.02 (d, J = 6.4 Hz, 2H), 3.96 (d, J = 12.4 Hz, 2H), 3.24- 3.23 (m, 1H), 2.74 (s, 2H), 2.02- 1.85 (m, 1H), 1.73 (d, J = 11.1Hz, 2H), 1.39 (s, 9H), 1.24- 1.02 (m, 2H).
 

Historical Records

Technical Information

Categories