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2-(6-Chloro-4-pyrimidinyl)-1,2,3,4-tetrahydroisoquinoline synthesis

1synthesis methods
-

Yield: 82%

Reaction Conditions:

with N-ethyl-N,N-diisopropylamine in isopropyl alcohol at 0 - 20; for 1 h;

References:

Bregman, Howard;Berry, Loren;Buchanan, John L.;Chen, April;Du, Bingfan;Feric, Elma;Hierl, Markus;Huang, Liyue;Immke, David;Janosky, Brett;Johnson, Danielle;Li, Xingwen;Ligutti, Joseph;Liu, Dong;Malmberg, Annika;Matson, David;McDermott, Jeff;Miu, Peter;Nguyen, Hanh Nho;Patel, Vinod F.;Waldon, Daniel;Wilenkin, Ben;Zheng, Xiao Mei;Zou, Anruo;McDonough, Stefan I.;Dimauro, Erin F. [Journal of Medicinal Chemistry,2011,vol. 54,# 13,p. 4427 - 4445] Location in patent:experimental part