Home Cart Sign in  
Chemical Structure| 207976-92-9 Chemical Structure| 207976-92-9

Structure of 207976-92-9

Chemical Structure| 207976-92-9

*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 [ 207976-92-9 ]

CAS No. :207976-92-9
Formula : C5H6ClNO
M.W : 131.56
SMILES Code : O=C1C(Cl)=CCCN1
MDL No. :MFCD18072446

Safety of [ 207976-92-9 ]

Application In Synthesis of [ 207976-92-9 ]

* 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 [ 207976-92-9 ]

[ 207976-92-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 27143-07-3 ]
  • [ 207976-92-9 ]
  • [ 503614-56-0 ]
YieldReaction ConditionsOperation in experiment
66.1% With triethylamine; In toluene; for 12h;Reflux; Under room temperature, the toluene (500 ml), 3-chloro -5,6-dihydro-pyridine -2 (1H)-one (35 g, crude), 2-chloro-2 - (2 - (4-methoxyphenyl) hydrazono) ethyl acetate (30.8 g, 0 . 120 mol) and triethylamine (24.2 g, 0 . 240 mol) are added to a reaction flask. The obtained mixture is heated to reflux under agitation, and the reaction to reflux 12 hours. The resultant mixture to cool to room temperature, into ethyl acetate (500 ml) and water (500 ml) in a mixed solution, filtered. The obtained filter cake drying under reduced pressure to get the yellow solid 25.0 g, that is, 1 - (4-methoxyphenyl) - 7-oxo -4, 5, 6, 7-tetrahydro -1H-pyrazolo [3,4-c] pyridine-3-carboxylic acid ethyl ester (yield: 66.1percent).
56% With triethylamine; In toluene; at 130℃; for 4h; General procedure: Toluene (1.55 dm3), 62 g 11 (0.471 mol), 242 g 3(0.943 mol), and 286 g triethylamine (2.828 mol) were sequentially charged at RT into a 3 dm3 three-neckedround-bottomed flask, fitted with a condenser, a mechanical stirrer, and a CaCl2 guard tube. The reaction mixture was refluxed at 130 °C for 4 h, cooled to RT, poured into930 cm3 ice cold water, and extracted with dichloromethane(4 9 930 cm3). The organic layers were combined, washed with brine (2 9 930 cm3), dried over anhydrous Na2SO4, and concentrated under reduced pressureat <55 °C. The crude material thus obtained was stirred with 620 cm3 MTBE for 1 h at RT, filtered, washedwith 310 cm3 MTBE, and finally dried at 45 C for 2 h toobtain 14 (83 g, 56percent, 99.3percent purity by HPLC analysis) as abrown solid. 1H NMR spectral data of 14 (see SupplementaryMaterial for details) was found to be consistent withthe values described in Ref. [15]
 

Historical Records

Technical Information

Categories