发明名称 Synthesis of chiral enaminones, their derivatives, and bioactivity studies thereof
摘要 This invention provides enantioenriched heterocyclic enaminone compounds with quaternary stereogenic centers and novel methods of preparing the compounds. Methods include the method for the preparation of a compound of formula (I):; comprising treating a compound of formula (II): ; with a transition metal catalyst under alkylation conditions.
申请公布号 US9518034(B2) 申请公布日期 2016.12.13
申请号 US201414514001 申请日期 2014.10.14
申请人 California Institute of Technology 发明人 Stoltz Brian M.;Dougherty Dennis A.;Duquette Douglas;Duffy Noah
分类号 C07D295/116;C07D209/88 主分类号 C07D295/116
代理机构 Foley Hoag LLP 代理人 Foley Hoag LLP ;Halstead David P.
主权项 1. A method for the preparation of a compound of formula (I):comprising treating a compound of formula (II):with a transition metal catalyst under alkylation conditions, wherein, as valence and stability permit, R1 and R2 are independently hydrogen or optionally substituted alkyl, aryl, aralkyl, heteroaryl, heteroaralkyl, alkenyl, or alkynyl; or R1 and R2 are taken together to form an optionally substituted heterocyclic ring; R3 is substituted or unsubstituted hydrogen, alkyl, aralkyl, aryl, heteroaralkyl, heteroaryl, alkenyl, alkynyl, or halo; R4 is hydrogen, halogen, alkyl, aralkyl, aryl, heteroaralkyl, heteroaryl, alkenyl, or alkynyl; R5, R6, R7, R8, R9, R10, R11, and R12 are independently selected for each occurrence from hydrogen, hydroxyl, halogen, nitro, alkyl, alkenyl, alkynyl, cyano, carboxyl, sulfate, amino, alkoxy, alkylamino, alkylthio, hydroxyalkyl, alkoxyalkyl, aminoalkyl, thioalkyl, ether, thioether, ester, amide, thioester, carbonate, carbamate, urea, sulfonate, sulfone, sulfoxide, sulfonamide, acyl, acyloxy, acylamino, aryl, heteroaryl, carbocyclyl, heterocyclyl, aralkyl, arylalkoxy, heteroaralkyl, carbocyclylalkyl, and heterocyclylalkyl; W is CR13R13, O, S, or NR14; R13 is selected, independently for each occurrence, from hydrogen, hydroxyl, halogen, nitro, alkyl, alkenyl, alkynyl, cyano, carboxyl, sulfate, amino, alkoxy, alkylamino, alkylthio, hydroxyalkyl, alkoxyalkyl, aminoalkyl, thioalkyl, ether, thioether, ester, amide, thioester, carbonate, carbamate, urea, sulfonate, sulfone, sulfoxide, sulfonamide, acyl, acyloxy, acylamino, aryl, heteroaryl, carbocyclyl, heterocyclyl, aralkyl, arylalkoxy, heteroaralkyl, carbocyclylalkyl, and heterocyclylalkyl; R14 is independently selected for each occurrence from hydrogen, alkyl, aryl, aralkyl, heteroaryl, heteroaralkyl, alkenyl, or alkynyl; wherein R2 and R4 may combine with the atoms to which they are attached to form an optionally substituted 4-9 membered heterocyclic ring, R4 and an occurrence of R13 may combine with the carbons to which they are attached to form an optionally substituted 3-8 membered ring, R4 and an occurrence of R14 may combine with the atoms to which they are attached to form an optionally substituted 4-8 membered heterocyclic ring, two occurrences of R13 may combine with the carbons to which they are attached to form a 3-8 membered ring, or an occurrence of R13 and an occurrence of R14 may combine with the atoms to which they are attached to form an optionally substituted 4-8 membered heterocyclic ring; and n is an integer from 1-4.
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