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ChemicalBook CAS DataBase List tert-Butyl 7-broMo-3,4-dihydroquinoline-1(2H)-carboxylate

tert-Butyl 7-broMo-3,4-dihydroquinoline-1(2H)-carboxylate synthesis

3synthesis methods
14548-39-1 Synthesis
6-Bromoindanone

14548-39-1
316 suppliers
$10.00/1g

-

Yield:-

Steps:

Multi-step reaction with 4 steps
1: hydroxylamine hydrochloride; potassium hydroxide / water; methanol / 3 h / Reflux
2: methanesulfonyl chloride; triethylamine / dichloromethane / 2 h / -15 °C
3: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / 20 °C
4: dmap; triethylamine / tetrahydrofuran / 60 °C

References:

Koehler, Michael F. T.;Bergeron, Philippe;Choo, Edna F.;Lau, Kevin;Ndubaku, Chudi;Dudley, Danette;Gibbons, Paul;Sleebs, Brad E.;Rye, Carl S.;Nikolakopoulos, George;Bui, Chinh;Kulasegaram, Sanji;Kersten, Wilhelmus J. A.;Smith, Brian J.;Czabotar, Peter E.;Colman, Peter M.;Huang, David C. S.;Baell, Jonathan B.;Watson, Keith G.;Hasvold, Lisa;Tao, Zhi-Fu;Wang, Le;Souers, Andrew J.;Elmore, Steven W.;Flygare, John A.;Fairbrother, Wayne J.;Lessene, Guillaume [ACS Medicinal Chemistry Letters,2014,vol. 5,# 6,p. 662 - 667]

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