Home Cart Sign in  
Chemical Structure| 868387-60-4 Chemical Structure| 868387-60-4

Structure of 868387-60-4

Chemical Structure| 868387-60-4

*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 [ 868387-60-4 ]

CAS No. :868387-60-4
Formula : C10H8N4S
M.W : 216.26
SMILES Code : NC1=NC(C2=CNC3=NC=CC=C32)=CS1
MDL No. :MFCD11180047

Safety of [ 868387-60-4 ]

Application In Synthesis of [ 868387-60-4 ]

* 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 [ 868387-60-4 ]

[ 868387-60-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 868387-60-4 ]
  • [ 1877-64-1 ]
  • C19H16N4O3S2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine; 1-(methanesulfonyl)-1H-1,2,3-benzotriazole; In tetrahydrofuran; at 160℃; for 0.166667h;Microwave irradiation; Sealed tube; General procedure: Compound 16 (216 mg, 1.0 mmol), phenylacetic acid (150 mg, 1.10 mmol) and N-(1-methanesulfonyl)benzotriazole (220 mg, 1.10 mmol) were placed in a microwave reaction vessel. TΗF (2 mL) was added followed by Et3N (0.5 mL, 3.59 mmol) and the mixture heated in the sealed tube at 160 C for 10 minutes. Upon cooling to RT the reaction was concentrated to l mL, and then MeCN was added (4mL) and the product 2-phenyl-N-[4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-thiazol-2-yl]-acetamide precipitated, was filtered, washed with acetonitrile and dried.
 

Historical Records