Home Cart Sign in  
Chemical Structure| 1427311-63-4 Chemical Structure| 1427311-63-4

Structure of 1427311-63-4

Chemical Structure| 1427311-63-4

*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 [ 1427311-63-4 ]

CAS No. :1427311-63-4
Formula : C27H31F3N4O10
M.W : 628.55
SMILES Code : O=C(NCC#CC1=CC([N+]([O-])=O)=C([C@@H](OCC2=CN([C@@H]3O[C@H](CO)[C@@H](O)C3)C(NC2=O)=O)C(C)(C)C)C=C1OC)C(F)(F)F
MDL No. :N/A

Safety of [ 1427311-63-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 1427311-63-4 ]

* 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.

  • Upstream synthesis route of [ 1427311-63-4 ]
  • Downstream synthetic route of [ 1427311-63-4 ]

[ 1427311-63-4 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 1427311-62-3 ]
  • [ 14719-21-2 ]
  • [ 1427311-63-4 ]
YieldReaction ConditionsOperation in experiment
90% With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine In N,N-dimethyl-formamide at 50℃; for 12 h; A solution of compound 61 (80 mg, 0.13 mmol), N-propargyltrifluoroacetylamide (196 mg, 1.30 mmol), tetrakis(triphenylphosphine)-palladium(0) (30 mg, 0.026 mmol), Cul (9.9 mg, 0.052 mmol), and Et3N (80 μΓ) in anhydrous DMF (3.0 mL) was stirred at 50°C for 12 hours. The mixture was concentrated in vacuo and the residue was purified by silica gel column chromatography to yield 5-{(5)-l-[5-methoxy-4-(3-trifluoroacetamido-l-propynyl)-2-nitrophenyl]-2,2-dimethyl-propyloxy}methyl-2'-deoxyuridine 62 (75 mg, 90percent). 1H NMR (400 MHz, MeOD-d4): 5 8.1 1 (s, 1 Η, Η-6), 8.08 (s, 1 Η, Ph-H), 7.36 (s, 1 H, Ph-H), 6.27 (t, 1 H, J = 6.4 Hz, Η-Γ), 5.33 (s, 1 H, Ph-CH), 4.47 (m, 1 H, H-3'), 4.44 (s, 2 H, 5-CH2), 4.32 (d, 2 H, J = 2.0 Hz, CH2), 4.08 (s, 3 H, OCH3), 3.99 (m, 1 H, H-4'), 3.87 (m, 1 H, H-5'a), 3.79 (m, 1 H, H-5'b), 2.30 (m, 2 H, H-2), 0.93 (s, 9 H, C(CH3)3).
References: [1] Patent: WO2013/40257, 2013, A1, . Location in patent: Page/Page column 152; 153; 154.
  • 2
  • [ 1028383-90-5 ]
  • [ 1427311-63-4 ]
References: [1] Patent: WO2013/40257, 2013, A1, .
  • 3
  • [ 766-85-8 ]
  • [ 1427311-63-4 ]
References: [1] Patent: WO2013/40257, 2013, A1, .
  • 4
  • [ 55215-55-9 ]
  • [ 1427311-63-4 ]
References: [1] Patent: WO2013/40257, 2013, A1, .
  • 5
  • [ 1427311-72-5 ]
  • [ 1427311-63-4 ]
References: [1] Patent: WO2013/40257, 2013, A1, .
  • 6
  • [ 1427311-75-8 ]
  • [ 1427311-63-4 ]
References: [1] Patent: WO2013/40257, 2013, A1, .
  • 7
  • [ 1427311-76-9 ]
  • [ 1427311-63-4 ]
References: [1] Patent: WO2013/40257, 2013, A1, .
 

Historical Records