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tert-Butyl 7-fluoro-6-nitro-3,4-dihydroisoquinoline-2(1H)-carboxylate synthesis

6synthesis methods
912878-83-2 Synthesis
7-Fluoro-6-nitro-1,2,3,4-tetrahydroisoquinoline

912878-83-2
20 suppliers
$45.00/10mg

24424-99-5 Synthesis
Di-tert-butyl dicarbonate

24424-99-5
820 suppliers
$13.50/25G

-

Yield:912846-67-4 76%

Reaction Conditions:

with triethylamine in 1,4-dioxane at 20;

References:

Watson, Nigel S.;Adams, Carl;Belton, David;Brown, David;Burns-Kurtis, Cynthia L.;Chaudry, Laiq;Chan, Chuen;Convery, Máire A.;Davies, David E.;Exall, Anne M.;Harling, John D.;Irvine, Stephanie;Irving, Wendy R.;Kleanthous, Savvas;McLay, Iain M.;Pateman, Anthony J.;Patikis, Angela N.;Roethke, Theresa J.;Senger, Stefan;Stelman, Gary J.;Toomey, John R.;West, Robert I.;Whittaker, Caroline;Zhou, Ping;Young, Robert J. [Bioorganic and Medicinal Chemistry Letters,2011,vol. 21,# 6,p. 1588 - 1592] Location in patent:scheme or table