Home Cart Sign in  
Chemical Structure| 625100-00-7 Chemical Structure| 625100-00-7

Structure of 625100-00-7

Chemical Structure| 625100-00-7

*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 [ 625100-00-7 ]

CAS No. :625100-00-7
Formula : C8H9BrN2
M.W : 213.07
SMILES Code : BrC1=CC2=C(N=C1)CCNC2
MDL No. :MFCD08059299

Safety of [ 625100-00-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of [ 625100-00-7 ]

* 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 [ 625100-00-7 ]

[ 625100-00-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 625100-00-7 ]
  • [ 24424-99-5 ]
  • [ 1184950-48-8 ]
YieldReaction ConditionsOperation in experiment
97.5% With triethylamine;dmap; In tetrahydrofuran; at 20℃; for 4h; Step 1: t-butyl 3-bromo-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate To a flask containing 3-bromo-5,6,7,8-tetrahydro-1,6-naphthyridine (1.50 g, 7.04 mmol), was added THF (70 mL, 863 mmol), di-tert-butyldicarbonate (1.77 g, 8.10 mmol), TEA (5.89 mL, 42.2 mmol), and DMAP (43.0 mg, 0.352 mmol). The solution was stirred at rt for 4 h. The solvent was then concentrated. To the resulting residue was added EtOAc (150 mL) and water (50 mL). After separation, the aqueous layer was extracted with EtOAc (2*150 mL). The combined organic layers were then washed with water (2*100 mL), brine (100 mL), dried (Mg2SO4), and concentrated to yield tert-butyl 3-bromo-7,8-dihydro-1,6-naphthyridine-6(5H)-carboxylate (2.15 g, 97.5%). LC-MS: (FA) ES+ 314; 1H NMR (Methanol-d4, 300 MHz) delta8.43 (s, 1H, 7.83 (s, 1H), 4.60 (s, 2H), 3.73 (t, J=6.0 Hz, 2H), 2.89 (t, J=6.0 Hz, 2H), 1.48 (s, 9H).
75% With triethylamine; In dichloromethane; at 20℃; To a stirred solution of 3-bromo-5,6,7,8-tetrahydro-l,6-naphthyridine (5.00 g, 23.4 mmol, 1.0 eq.) and Di-tert-butyl pyrocarbonate (BOG20, 6.14 g, 28.1 mmol, 1.2 eq.) in (0151) dichloromethane (50 ml) was added triethylamine (2.30 g, 23.4 mmol, 1.0 eq.), and the resultant mixture was stirred at ambient temperature overnight. The reaction mixture was concentrated to dryness, and the crude material was purified by a column chromatography (200-300 mesh silica gel, PE/E A = 5/1) to afford tert-butyl 3-bromo-7,8-dihydro-l,6-naphthyridine-6(5H)-carboxylate (5.50 g, 75% yield) as a colorless oil. 1 HNMR (400 MHz, CDC13) 5(ppm) 8.48 (d, 1H), 7.57 (d, (0152) 1H), 4.59 (s, 2H), 3.75 (t, 2H), 2.96 (t, 2H), 1.50 (s, 9H).
 

Historical Records

Technical Information

Categories