Home Cart Sign in  
Chemical Structure| 1300582-43-7 Chemical Structure| 1300582-43-7

Structure of 1300582-43-7

Chemical Structure| 1300582-43-7

*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 [ 1300582-43-7 ]

CAS No. :1300582-43-7
Formula : C13H15BrN2O2
M.W : 311.17
SMILES Code : O=C(N1N=C(C)C2=C1C=C(Br)C=C2)OC(C)(C)C
MDL No. :MFCD24471372

Safety of [ 1300582-43-7 ]

Application In Synthesis of [ 1300582-43-7 ]

* 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 [ 1300582-43-7 ]

[ 1300582-43-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 7746-27-2 ]
  • [ 1300582-43-7 ]
YieldReaction ConditionsOperation in experiment
75% With triethylamine;dmap; In dichloromethane; at 0℃; for 3h; To a solution of 6- bromo-3 -methyl- lH-indazole (330 mg, 1.56 mmol) in dichloromethane (15 mL) was added triethylamine (0.67 mL, 4.68 mmol), di-tert-butyl dicarbonate (443 mg, 2.03 mmol) and 4- (dimethylamino)pyridine (19 mg, 0.156 mmol) at 0 C. The resulting solution was stirred for 3 h and the reaction mixture was washed with water, was dried over magnesium sulfate, was filtered and was concentrated. The residue was purified by column chromatography (eluted with ethyl acetate:hexanes = 1 :6) to give tert-butyl 6-bromo-3 -methyl- 1 H-indazole- 1- carboxylate (366 mg, 75% yield) as a light pink solid. ¾ NMR (400 MHz, CDC13): delta 8.31 (s, 1H), 7.46 (d, 1H), 7.37 (d, 1H), 2.54 (s, 3H), 1.60 (s, 9H).
70% Intermediate 96 tert-butyl <strong>[7746-27-2]6-bromo-3-methyl-1H-indazole</strong>-1-carboxylate To a solution of intermediate 95 (10.0 g, 47.39 mmoles) in acetonitrile (100 ml) cooled to 20 C., Boc-anhydride (10.3 g, 34.09 mmoles) was added followed by DMAP (0.579 g, 4.73 mmoles) and triethylamine (4.7 g, 47.39 mmoles) and the reaction mixture was stirred at room temperature. After 12 h, the reaction mixture was concentrated and quenched with water and solid precipitated was filtered and dried under vacuum to afford the title compound as colourless solid (10.3 g, 70% yield). 1H-NMR (delta ppm, DMSO-d6, 400 MHz): delta 8.19 (d, J=1.2 Hz, 1H), 7.81 (d, J=8.4 Hz, 1H),), 7.54 (dd, J=8.5, 1.7 Hz, 1H), 2.50 (s, 3H), 1.62 (s, 9H).
 

Historical Records

Technical Information

Categories