Home Cart Sign in  
Chemical Structure| 1253189-14-8 Chemical Structure| 1253189-14-8

Structure of 1253189-14-8

Chemical Structure| 1253189-14-8

*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 [ 1253189-14-8 ]

CAS No. :1253189-14-8
Formula : C11H8ClF2NO2
M.W : 259.64
SMILES Code : FC1=C(C2CC(C(CCl)=O)=NO2)C(F)=CC=C1

Safety of [ 1253189-14-8 ]

Application In Synthesis of [ 1253189-14-8 ]

* 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 [ 1253189-14-8 ]

[ 1253189-14-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 214834-18-1 ]
  • [ 1253189-14-8 ]
  • tert-butyl 4-(4-(5-(2,6-difluorophenyl)-4,5-dihydroisoxazol-3-yl)thiazol-2-yl)piperidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
89% In methanol; for 4h;Reflux; Step c: Put it into a 250mL pear-shaped bottle,Add magnets one by one,The compound represented by formula (2-3) (38.51 mmol),100mL anhydrous methanol,Add 4-aminothiocarbonyltetrahydropyridine-1(2H)-carboxylic acid tert-butyl ester (38.02mmol, 1eq.) under stirring,Warm up to reflux,The reaction was completed in about 4 hours.Concentrate under reduced pressure to remove most of the methanol,Add 100mL water,Extract with ethyl acetate,Separate the liquids, dry the organic phase with anhydrous sodium sulfate,Filter, concentrate the filtrate,Purified by silica gel column chromatography to obtain the compound represented by formula (2-4),The yield (based on 4-aminothiocarbonyltetrahydropyridine-1(2H)-carboxylic acid tert-butyl ester) was 89%.
With sodium bromide; In acetone; for 12h;Reflux; (3) Compound (1 mol) represented by formula (2-3),4-aminothiocarbonyltetrahydropyridine-1 (2H) -tert-butyl formate(1.1 mol) and sodium bromide (0.1 mol) were sequentially added to 2.5 L of acetone,The reaction system was heated under reflux for 12 h. After the reaction was completed, acetone was removed, 2 L of water was added, and the mixture was extracted with 500 mL * 3 ethyl acetate. The organic phases were combined, dried and concentrated to obtain the crude compound of formula (2-4). The elution system formed by silica gel with petroleum ether and ethyl acetate was purified by column chromatography, and the pure compound of formula (2-4) was finally obtained;
With sodium bromide; In acetone; for 12h;Reflux; (3) The compound represented by formula (2-5) (1mol), 4-aminothiocarbonyl tetrahydropyridine-1(2H)-t-butyl formate (1.1mol) and sodium bromide (0.1mol) in sequence Add to 2.5L of acetone, the reaction system is heated and refluxed for 12h, after the reaction is complete, remove the acetone, add 2L of water, extract with 500mL*3 ethyl acetate, combine the organic phases, dry and concentrate to obtain the formula (2-6) The crude product of the compound is further purified by column chromatography with an elution system formed by silica gel, petroleum ether and ethyl acetate to finally obtain the pure product of the compound represented by formula (2-6)
 

Historical Records