Home Cart Sign in  
Chemical Structure| 1182728-10-4 Chemical Structure| 1182728-10-4

Structure of 1182728-10-4

Chemical Structure| 1182728-10-4

*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 [ 1182728-10-4 ]

CAS No. :1182728-10-4
Formula : C19H21NO2S
M.W : 327.44
SMILES Code : O=C1N(C2=CC=CC(SCC3=CC=CC=C3)=C2CC)CCOC1
MDL No. :MFCD27991762

Safety of [ 1182728-10-4 ]

Application In Synthesis of [ 1182728-10-4 ]

* 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 [ 1182728-10-4 ]

[ 1182728-10-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 109-11-5 ]
  • [ 1182728-08-0 ]
  • [ 1182728-10-4 ]
YieldReaction ConditionsOperation in experiment
85% With potassium carbonate;copper(l) iodide; N,N`-dimethylethylenediamine; In toluene; at 110℃; for 20h;Inert atmosphere; 1.5) 4-(3-Benzylsulfanyl-2-ethyl-phenyl)-<strong>[109-11-5]morpholin-3-one</strong> (Intermediate 5): <n="48"/>Intermediate 4 (1.075 g, 3.5 mmol), <strong>[109-11-5]morpholin-3-one</strong> (389 mg, 3.85 mmol), CuI (67 mg, 0.35 mmol), N,N'-dimethylethylene diamine (75 μl, 0.7 mmol) and K2CO3 (1 ,064 g, 7.7 mmol) were suspended in toluene (30 ml) under argon and heated to 110 C for 2Oh. After cooling to RT the reaction mixture was quenched by addition of 100 ml sat. aq. NH4CI, 150 ml concentrated NH3 in water and 100 ml water and extracted three times with ethyl acetate. The organic layers were combined and washed with water and sat. aq. NaCI-solution, dried with MgSO4, filtered and evaporated to dryness. The resulting011 crystallizes upon standing and was triturated with n-heptane-MTBE (19:1). Yield: 974 mg, 85 %
85% With potassium carbonate;copper(l) iodide; N,N`-dimethylethylenediamine; In toluene; at 110℃; for 20h;Inert atmosphere; 1.6) 4-(3-Benzylsulfanyl-2-ethyl-phenyl)-<strong>[109-11-5]morpholin-3-one</strong> (Intermediate 6): Intermediate 5 (1.075 g, 3.5 mmol), <strong>[109-11-5]morpholin-3-one</strong> (389 mg, 3.85 mmol), CuI (67 mg, 0.35 mmol), N,N'-dimethylethylene diamine (75 μl, 0.7 mmol) and K2CO3 (1 ,064 g , 7.7 mmol) were suspended in toluene (30 ml) under argon and heated to 1100C for 20 h. After cooling to RT the reaction mixture was quenched by addition of 100 ml sat. aq NH4CI, 150 ml cone. NH3 in water and 100 ml water and extracted three times with ethyl acetate. The organic layers were combined and washed with water and sat. aq NaCI-solution, dried with MgSO4, filtered and evaporated to dryness. The resulting oil crystallizes upon standing and was triturated with n-heptane-MTBE (19:1). Yield: 974 mg, 85 %
 

Historical Records

Technical Information

Categories