Home Cart Sign in  
Chemical Structure| 159503-92-1 Chemical Structure| 159503-92-1

Structure of 159503-92-1

Chemical Structure| 159503-92-1

*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 [ 159503-92-1 ]

CAS No. :159503-92-1
Formula : C17H25NO2S
M.W : 307.45
SMILES Code : O=C(N1CCC(SCC2=CC=CC=C2)CC1)OC(C)(C)C
MDL No. :N/A

Safety of [ 159503-92-1 ]

Application In Synthesis of [ 159503-92-1 ]

* 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 [ 159503-92-1 ]

[ 159503-92-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 100-39-0 ]
  • [ 134464-79-2 ]
  • [ 159503-92-1 ]
YieldReaction ConditionsOperation in experiment
97% With potassium carbonate; In N,N-dimethyl-formamide; at 70℃; for 60h; Preparation of tert-butyl 4-(benzylthio)piperidine-l-carboxylate. A solution of tert-butyl 4-mercaptopiperidine-l-carboxylate (211.2 mg, 0.9718 mmol) and benzyl bromide (199.5 mg, 1.166 mmol) in DMF (3.9 mL) was treated with potassium carbonate (537.2 mg, 3.887 mmol). The reaction mixture was stirred at 70C for 60 h. After cooling to ambient temperature, the reaction mixture was diluted with EtOAc and washed successively with water and saturated NaCl(aq). The combined organic extracts were concentrated in vacuo, and the residue was purified by silica chromatography (1-50% EtOAc in hexanes as the gradient eluent) to afford the title compound (290.1 mg, 0.9436 mmol, 97% yield) in sufficient purity for step 2. MS (apci) m/z = 208.1 (M+H-Boc).
97% With potassium carbonate; In N,N-dimethyl-formamide; at 70℃; for 60h; Preparation of tert-butyl 4-(benzylthio)piperidine-l-carboxylate. To a solution of tert-butyl 4-mercaptopiperidine-l-carboxylate (211 mg, 0.97 mmol) and Benzyl bromide (200 mg, 1.17 mmol) in DMF (3.9 mL) was added potassium carbonate (537 mg, 3.89 mmol). The reaction mixture was stirred 60 h at 70C. After cooling to ambient temperature, the reaction mixture was diluted with EtOAc and washed with water and brine. The organic extracts were concentrated in vacuo. The residue was purified using silica chromatography (1- 50 % EtOAc in Hexanes as the gradient eluent) to afford the title compound (290 mg, 97 % yield) in sufficient purity for step 2. MS (apci) m/z = 208.1 (M-Boc).
 

Historical Records