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(4-propan-2-yloxyphenyl)-pyridin-3-ylmethanone synthesis

4synthesis methods
95091-91-1 Synthesis
N-Methoxy-N-methylnicotinamide

95091-91-1
43 suppliers
$60.00/50mg

(4-propan-2-yloxyphenyl)-pyridin-3-ylmethanone

1094639-27-6
0 suppliers
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Yield:1094639-27-6 21%

Reaction Conditions:

Stage #1: 1-bromo-4-isopropoxybenzenewith n-butyllithium in diethyl ether;hexane at -78; for 1 h;Inert atmosphere;Cooling with acetone-dry ice;
Stage #2: N-methoxy-N-methylpyridine-3-carboxamide in tetrahydrofuran;diethyl ether;hexane at -78 - 20; for 4.5 h;Inert atmosphere;Cooling with acetone-dry ice;

References:

Keenan, Martine;Abbott, Michael J.;Alexander, Paul W.;Armstrong, Tanya;Best, Wayne M.;Berven, Bradley;Botero, Adriana;Chaplin, Jason H.;Charman, Susan A.;Chatelain, Eric;Von Geldern, Thomas W.;Kerfoot, Maria;Khong, Andrea;Nguyen, Tien;McManus, Joshua D.;Morizzi, Julia;Ryan, Eileen;Scandale, Ivan;Thompson, R. Andrew;Wang, Sen Z.;White, Karen L. [Journal of Medicinal Chemistry,2012,vol. 55,# 9,p. 4189 - 4204] Location in patent:supporting information; experimental part