1217809-88-5Relevant academic research and scientific papers
Hydroxoiridium-Catalyzed Hydroalkylation of Terminal Alkenes with Ureas by C(sp3)?H Bond Activation
Yamauchi, Daisuke,Nishimura, Takahiro,Yorimitsu, Hideki
, p. 7200 - 7204 (2017)
Direct alkylation of a methyl group, on di- and trisubstituted ureas, with terminal alkenes by C(sp3)?H bond activation proceeded in the presence of a hydroxoiridium/bisphosphine catalyst to give high yields of the corresponding addition products. The hydroxoiridium/bisphosphine complex generates an amidoiridium intermediate by reaction with ureas having an N?H bond.
Hydrochloric cinacalcet preparation method
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, (2017/08/29)
The invention discloses a hydrochloric cinacalcet preparation method. Commercial m-(trifluoromethyl) acetophenone, formaldehyde, (R)-1-(1-naphthyl) ethylamine and the like serve as raw materials, an intermediate (R)-3-(1-(naphthalene-1-base) ethyl amino)-1-(3-(trifluoromethyl) phenyl) propane-1-ketone is prepared by multi-component Mannich reaction and subjected to reduction reaction to prepare cinacalcet, and the cinacalcet reacts with hydrochloric acid, so that hydrochloric cinacalcet can be prepared. The preparation method is short in synthetic route, low in raw material cost, low in price, safe in normal pressure reaction operation and suitable for large-scale production and has good social and economic benefits, and metal zinc amalgam reducing agents are used. Experiments prove that the recrystallization yield of the cinacalcet can reach 93.4% or more, the purity of the cinacalcet can reach 99.6% or more, the yield of the hydrochloric cinacalcet can reach 94.2% or more, and the purity of the hydrochloric cinacalcet can reach 99.7% or more.
