Home Cart Sign in  
Chemical Structure| 897031-20-8 Chemical Structure| 897031-20-8

Structure of 897031-20-8

Chemical Structure| 897031-20-8

*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 [ 897031-20-8 ]

CAS No. :897031-20-8
Formula : C9H7N3O
M.W : 173.17
SMILES Code : OC1=NC=CC(C2=CC=CN=C2)=N1

Safety of [ 897031-20-8 ]

Application In Synthesis of [ 897031-20-8 ]

* 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 [ 897031-20-8 ]

[ 897031-20-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 897031-20-8 ]
  • [ 483324-01-2 ]
YieldReaction ConditionsOperation in experiment
65% With thionyl chloride; N,N-dimethyl-formamide; at 70℃; for 6h; (2) Feeding: Weigh 2-oxo-4- (3-pyridyl) - pyrimidine and 1.73g thionyl chloride 20.0ml into the reaction flask and catalyst DMF770muL, system reaction 6h after TLC monitoring material point at 70 disappeared, the reaction was completed.Post-treatment: the system to be cooled, the system was poured into 400ml of ice water, adjusted to pH 8 with sodium hydroxide solution, (30ml × 3) and extracted with ethyl acetate, the extract was dried over anhydrous sodium sulfate, suction filtered, the The filtrate was evaporated to dryness to give a pale yellow solid, yield 65%.
56% With trichlorophosphate; at 50℃; for 4.5h; 2. Preparation of 2-chloro-4-(3-pyridyl)-pyrimidine In a 250 ml two necked flask, equipped with a mechanical stirrer and a condenser, a mixture of 2-oxo-4-(3-pyidyl)-pyrimidine (3 g, 0.017 mol) and POCl3 (18 ml) was stirred at 50 C. for 4.5 hrs. The reaction mixture was poured into cold water (50 ml) and neutralized with 47% aqueous NaOH solution to pH 8. The solution was extracted with ethyl acetate (2*50 ml). The combined ethyl acetate phase was dried over magnesium sulfate and evaporated to dryness to give 2-chloro-4-(3-pyridyl)-pyrimidine in 56% yield, having a purity of 97%.
520 g With trichlorophosphate; In toluene; for 5h;Reflux; In a 5000 mL round bottom flask, add 1300 mL of toluene.Then, 500 g of 4-(pyridinyl-3-yl)pyrimidine-2(H)-one was added and stirred at room temperature for 20 minutes.Slowly add 532g of phosphorus oxychloride, heat to a slight reflux, and stir for 5 hours.After the TLC detection material completely disappeared, the reaction solution was cooled to room temperature.Then the reaction solution was poured into 3,500 mL of ice water.Adding organic solvent to dichloromethane, extracting three times, and combining the organic phases,Then concentrated and separated by column chromatography to obtain pure2-chloro-4-(pyridin-3-yl)pyridine 520g.
 

Historical Records

Technical Information

Categories