Home Cart Sign in  
Chemical Structure| 88093-48-5 Chemical Structure| 88093-48-5

Structure of 88093-48-5

Chemical Structure| 88093-48-5

*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 [ 88093-48-5 ]

CAS No. :88093-48-5
Formula : C8H11ClN2O2
M.W : 202.64
SMILES Code : O=C1C(Cl)=C(O)C=NN1C(C)(C)C

Safety of [ 88093-48-5 ]

Application In Synthesis of [ 88093-48-5 ]

* 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 [ 88093-48-5 ]

[ 88093-48-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 302348-51-2 ]
  • [ 88093-48-5 ]
  • 2-(tert-butyl)-4-chloro-5-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)oxy)pyridazin-3(2H)-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
31.3% With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20℃; A solution of 2-(tert-butyl)-4-chloro-5-hydroxypyridrazin-3(2H)-one (0.537 g, 2.65 mmol) in tetrahydrofuran (22.1 mL) was successively treated with <strong>[302348-51-2](4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol</strong> (0.745 g, 3.18 mmol), triphenylphosphine (1.04 g, 3.97 mmol), and diisopropylazodicarboxylate (0.782 mL, 3.97 mmol) at ambient temperature. After 45 min, the resulting mixture was diluted with water (20 mL), the aqueous layer separated then extracted with ethyl acetate (3*50 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The crude material was suspended in diethyl ether, stirred 3 h then collected by filtration and purified by silica gel chromatography using 4:1 hexane/ethyl acetate to afford the desired product as a white solid (0.347 g, 31.3percent yield). 1H NMR (300 MHz, DMSO-d6): delta 8.22 (s, 1H), 7.73 (d, J=8.0 Hz, 2H), 7.47 (d, J=8.0 Hz, 2H), 5.49 (s, 2H), 1.57 (s, 9H), 1.30 (s, 12H); 13C NMR (75 MHz, DMSO-d6, partial): delta 157.7, 153.5, 138.6, 134.7, 126.9, 125.1, 115.6, 83.7, 71.1, 65.3, 27.4, 24.6; HRMS-TOF (m/z): [M+Na]+ HRMS: Calcd. for C21H28B35ClN2O4: 419.1907. found 419.1903.
31.3% With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20℃; for 0.75h; 2-(t-butyl)-4-chloro-5-hydroxypyridazin-3(2H)-one (0.537 g, 2.65 mmol) to a solution in tetrahydrofuran (22.1 ml) of (4-(4,4,5,5-tertramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol (0.745g, 3.18mmol), triphenylphosphine (1.04g, 3.97mmol) and diisopropyl azodicarboxylate (0.782mL, 3.97mmol) was treated sequentially at ambient temperature by. After 45 minutes, the mixture is diluted with water (20 ml), by separating the water layer, then, extracted with ethyl acetate (3×50mL). In combination with an organic layer is dried sodium sulfate, filtration, concd. under decompression. Coarse material suspended in diethyl ether, 3 time and then, subsequently, recovered by filtration, 4:1 Phenylbicyclohexane/ethyl acetate are purified by silica gel chromatography using, as solid white to obtain a desired product (0. 347g, 31. 3percent yield).1H NMR (300MHz, DMSO-d6): delta8. 22 (s, 1H), 7. 73 (d, J = 8. 0Hz, 2H), 7. 47 (d, J = 8. 0Hz, 2H), 5. 49 (s, 2H), 1. 57 (s, 9H), 1. 30 (s, 12H);13C NMR (75MHz, DMSO-d6, part): delta157. 7,153. 5,138. 6,134. 7,126. 9,125. 1,115. 6, 83. 7, 71. 1, 65. 3, 27. 4, 24. 6 ; HRMS-TOF(m/z) : [M+Na]+HRMS: C21H28B35ClN2O4calculated value to: 419. 1907, actual value 419. 1903.
 

Historical Records

Technical Information

Categories