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Imidazopirrolidinona compounds
专利权人:
NOVARTIS AG
发明人:
ROBERT MAH,LIANG MAO,KEIICHI MASUYA,ACHIM SCHLAPBACH,STEFAN STUTZ,ANDREA VAUPEL,LV LIAO,PASCAL FURET,VITO GUAGNANO,PHILIPP HOLZER,JOERG KALLEN
申请号:
ARP130100227
公开号:
AR089807A1
申请日:
2013.01.25
申请国别(地区):
AR
年份:
2014
代理人:
摘要:
1. Compounds used to treat disorders or diseases caused by MDM2 and / or MDM4 activities, and compounds containing these compounds. Current compounds are used as antitumor agents. 1. Characteristic 1: compound (1) of formula or salt (2) selected from formula;B from a set of formulas (3);Each R1 R1 is selected independently from halogen and methyl; R2 is selected from chlorine, fluorine, trifluoromethyl, methyl and cyanogen; R3 is selected from isopropyl, cyclopropene, isobutyl, cyclopentanediol and cyclopentanediol, or R3 is a residual formula (4),There, from Oh, oc832323,NH.8322;NHMe, NMe₂,Nhme and nhcoh; r83088 were selected from formula group (5);R83099a is independently selected from oc832323;CH₂CH₃,OH, OCF₃ and H; R¹⁶ is selected from H, -O-C₁₋₄ alkyl,halo, OCF₃,CN -C (O) NR R-C (O) -morfolinil-4-ilo hidroxi-azetidin-1-il-carbonilo -CH NR R-CH NR -C (O) RCh8322; CN, methyl picolinate -,-CH C (O) NR R-Ch8322; (c) (o) oh - (o) oh -, CH 8322; C (o) o-tar c831832421;-N(R⁹)-C(O)-alquilo C₁₋₄,-NR⁹R¹⁰ and C₁₋₄ alkyl optionally substituted by 1 or 2 OH; R¹⁷ is selected from H, -O-C₁₋₄ alkyl,-CH C (O) NR R-CH₂C (O) O-C₁₋₄ alkyl,-CH C (O) OH -NR R-C (o) No. 8313; r83044,-CH₂NR⁹R¹⁰,-C (o) oc8323y-ch8322; CN; R 831222 was selected from h, - o-coking c833218331s 832424;Oh, ch8322283; nr8313; r183044;-No. 8313; r83044 and azetidin-1-ilo, replaced by Oh or two ch8323y and oh; r8313 was selected from h-o-aquilo c83318324;1. Lease of c83218331 and 83242431;-8313; 830404;-N(R⁹)-C(O)alquilo C₁₋₄ y -C(O)NR⁹R¹⁰;R83044 from h, ch8323y-ch8322; - ch832323;R2 1 was selected from - No. 83013; R1 830404;-CH₂NR⁹R¹⁰,C (o) nr8313; r83044 and CN; r83099 were selected from the following aspects: H, isoacrylonitrile-c (o) - (ch8322245)C₁₋₄- alkyl,said C₁₋₄ alkyl optionally substituted by 1 or 2 substituents independently selected from OH, = O, heterocyclyl¹-C₁₋₄- alkyl,wherein said heterocyclyl¹-C₁₋₄-alkyl is optionally substituted by 1 or 2 OH, and said heterocyclyl¹ may be optionally substit
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