A Convenient Synthesis of (Z)-3- (a-Cyano-a-alkoxycarbonylmethylene)-2-piperazinones and Their Derivatives
摘要:
(Z)-3-(alpha-Cyano-alpha-alkoxycarbonylmethylene)-2-piperazinone derivatives (3) and trans-(Z)-3-(alpha-cyano-alpha-alkoxycarbonylmethylene)-octahydro-2 (1H)-quinoxalinone derivatives (5) possessing various alkoxycarbonyl groups are prepared directly from the reaction of dialkyl (E)-2,3-dicyanobutenedioates (1) with ethylenediamine (2) and with trans-1,2-diaminocyclohexane (4), respectively. Furthermore, cis-1,2-diaminocycloheptane (6) and meso-2,3-diaminobutane (8) were reacted with the diethyl ester Ib to give cis-(Z)-3-(alpha-cyano-alpha-ethoxycarbonyl-methylene)decahydro-2H-cycloheptapyrazin-2-one (7) and cis-(Z)-3-(alpha-cyanoyano-alpha-ethoxycarbonylmethylene)-5,6-dimethyl-2-piperazinone (9), respectively. The structural studies of 3, 5, 7, and 9 were carried out by NMR experiments in some details.
[EN] PYRAZOLOPYRIMIDINE INHIBITORS OF IRAK4 ACTIVITY<br/>[FR] INHIBITEURS DE L'ACTIVITÉ D'IRAK4 À BASE DE PYRAZOLOPYRIMIDINE
申请人:MERCK SHARP & DOHME
公开号:WO2016144846A1
公开(公告)日:2016-09-15
The present invention relates to pyrazolopyrimidine inhibitors of IRAK4 of formula (I) and provides compositions comprising such inhibitors, as well as methods therewith for treating IRAK4-mediated or -associated conditions or diseases.
Hetrocyclic compounds that are inhibitors of the enzyme DPP-IV
申请人:——
公开号:US20030199528A1
公开(公告)日:2003-10-23
The present invention relates to therapeutically active and selective inhibitors of the enzyme DPP-IV, pharmaceutical compositions comprising the compounds and the use of such compounds for and the manufacture of medicaments for treating diseases that are associated with proteins that are subject to inactivation by DPP-IV, such as type 2 diabetes and obesity. The present inhibitors are novel purine derivatives, attached at position 8 of the purine skeleton to a diamine.
Process for the preparation of nonracemic syn-1-(4-hydroxy-phenyl)-2-(4-hydroxy-4-phenyl -piperidin-1-yl)-1-propanol compounds
申请人:DSM CATALYTICA PHARMACEUTICALS, INC.
公开号:US20030144521A1
公开(公告)日:2003-07-31
The present invention provides a process for the preparation of a nonracemic diastereomer of 1-(4-benzoxy-phenyl)-2-(4-hydroxy-4-phenyl-piperidin-1-yl)-1-propanol by hydrogenation of a corresponding nonracemic 1-(4-benzoxy-phenyl)-2-(4-hydroxy-4-phenyl-piperidin-1-yl)-1-propanone using a catalyst system comprising ruthenium, a nonracemic diphosphine ligand, a bidentate amine ligand selected from amino-thioethers and achiral diamines, and a base.
The invention relates a compound represented by the formula (1):
Q
1
-Q
2
-C(═O)—N(R
1
)-Q
3
-N(R
2
)-T
1
-Q
4
(
1
)
wherein R
1
and R
2
represent H or the like; Q
1
represents an aromatic ring, heterocyclic ring or the like; Q
2
represents a single bond, aromatic ring, heterocyclic ring or the like; Q
3
represents a group
1
or the like, Q
4
represents an aromatic ring, heterocyclic ring or the like; and T
1
represents —CO— or —SO
2
—, and a medicine which comprises the compound and is useful for thrombosis and embolism.