Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

2,3-Butanoquinazoline-4(3H)-one synthesis

11synthesis methods
-

Yield:2446-62-0 92%

Reaction Conditions:

with potassium tert-butylate in tetrahydrofuran at 20;Inert atmosphere;

Steps:

Synthesis of 2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-ones: general procedure B

General procedure: Toasolutionoftheappropriatesubstituted2-(4-chlorobutanamido)-benzamidessubstrate(1.0eq)inTHF(10mLpermmolsubstrate)wasaddedtBuOK(2.0eq).ThereactionwasstirredatroomtemperatureuntilTLCindicatedcompletion,thensolventwasremovedinvacuo,theresultingresiduere-dissolvedinCH2Cl2(20mL)andNaHCO3(15mL),andtheaqueouslayerextractedwithCH2Cl2(520mL).ThecombinedorganicphasesweredriedoverMgSO4andsolventremovedinvacuo.TheproductswereobtainedafterpurificationoftheresiduebyFCC.

References:

Sutherell, Charlotte L.;Ley, Steven V. [Synthesis,2017,vol. 49,# 1,art. no. SS-2016-Z0435-OP,p. 135 - 144] Location in patent:supporting information