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(+/-)-(E)-4,5-dihydro-N-[4-(1-oxo-3-phenyl-2-propenyl)phenyl]-3-(3-pyridinyl)-5-isoxazolecarboxamide | 264605-89-2

中文名称
——
中文别名
——
英文名称
(+/-)-(E)-4,5-dihydro-N-[4-(1-oxo-3-phenyl-2-propenyl)phenyl]-3-(3-pyridinyl)-5-isoxazolecarboxamide
英文别名
N-[4-[(E)-3-phenylprop-2-enoyl]phenyl]-3-pyridin-3-yl-4,5-dihydro-1,2-oxazole-5-carboxamide
(+/-)-(E)-4,5-dihydro-N-[4-(1-oxo-3-phenyl-2-propenyl)phenyl]-3-(3-pyridinyl)-5-isoxazolecarboxamide化学式
CAS
264605-89-2
化学式
C24H19N3O3
mdl
——
分子量
397.433
InChiKey
INCXUIMDDUKCMH-MDWZMJQESA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    80.6
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • 4,5-Dihydro-isoxazole derivatives and their pharmaceutical use
    申请人:——
    公开号:US20040019059A1
    公开(公告)日:2004-01-29
    The present invention is concerned with the compounds of formula 1 wherein m, n and p are each independently 0 or 1 and q is 0, 1, 2, 3, 4 or 5; -A 1 =A 2 -A 3 =A 4 - is a pyridinylidene, pyridazinylidene, pyrimidinylidene, pyrazinylidene or phenylidene; B represents an amide, ketone or oxadiazole; D represents Ar or Het; Q represents a covalent direct bond or a ketone, —N—, —O—, —CR 5 R 6 —, amide, ethenyl, imine, sulfonyl, sulfinyl, 3-oxobutenyl, pyrazole, isoxazole or thiazole; L represents Ar or Het; R 1 represents hydrogen, halo, hydroxy, C (2-6) alkenyl, C (2-6) alkynyl, C (3-6) cycloalkyl, C (3-6) cycloalkenyl, cyano, guanidine, nitro, NR 17 R 18 , an optionally substituted C (1-6) alkyl or C (I6) alkyloxy; R 2 and R 3 each independently represent hydrogen, halo, C (1-6) alkyloxy or an optionally substituted C (1-6) alkyl; R 5 and R 6 each independently represent hydrogen, hydroxy, halo, an optionally substituted C (1-6) alkyl, C (2-6) alkenyl, C (2-6) alkynyl, C (3-6) cycloalkyl, C (3-6) cycloalkenyl, C (1-6) alkyloxy, cyano, (C═O)R 25 , (C—O)OR 16 , (SO 2 )R 16 , aminocarbonyloxy, aminoC (1-6) alkyl, NR 17 R 18 , N 3 , Ar or Het; or R 5 and R 6 together with the carbon atom to which they are attached, form an Ar or Het; Ar represents an optionally substituted C (6-14) aryl; Het represents an optionally substituted C (1-14) heterocycle; or a N-oxide, pharmaceutically acceptable addition salt, quaternary amine or stereochemically isomeric form thereof; the processes for their preparation and compositions comprising them. It further relates to their use as a medicine.
    本发明涉及公式1的化合物,其中m、n和p各自独立地为0或1,q为0、1、2、3、4或5;-A1=A2-A3=A4-为吡啶基亚甲基、吡嗪基亚甲基、嘧啶基亚甲基、吡嗪基亚甲基或苯基亚甲基;B代表酰胺、酮或噁二唑;D代表Ar或Het;Q代表共价直接键或酮、-N-、-O-、-CR5R6-、酰胺、乙烯基亚胺、磺酰基、亚磺酰基、3-氧代丁烯基、吡唑、异唑或噻唑;L代表Ar或Het;R1代表氢、卤素、羟基、C(2-6)烯基、C(2-6)炔基、C(3-6)环烷基、C(3-6)环烯基、基、鸟氨酸基、硝基、NR17R18、可选取代的C(1-6)烷基或C(I6)烷氧基;R2和R3各自独立地代表氢、卤素、C(1-6)烷氧基或可选取代的C(1-6)烷基;R5和R6各自独立地代表氢、羟基、卤素、可选取代的C(1-6)烷基、C(2-6)烯基、C(2-6)炔基、C(3-6)环烷基、C(3-6)环烯基、C(1-6)烷氧基、基、(C═O)R25、(C-O)OR16、(SO2)R16、基羰氧基、基C(1-6)烷基、NR17R18、N3、Ar或Het;或者R5和R6与它们连接的碳原子一起形成Ar或Het;Ar代表可选取代的C(6-14)芳基;Het代表可选取代的C(1-14)杂环;或者它们的N-氧化物、药学上可接受的加合盐、季盐或立体化学异构体形式;以及它们作为药物的用途。
  • 4,5-DIHYDRO-ISOXAZOLE DERIVATIVES AND THEIR PHARMACEUTICAL USE
    申请人:JANSSEN PHARMACEUTICA N.V.
    公开号:EP1119568A1
    公开(公告)日:2001-08-01
  • US6583141B1
    申请人:——
    公开号:US6583141B1
    公开(公告)日:2003-06-24
  • US7414048B2
    申请人:——
    公开号:US7414048B2
    公开(公告)日:2008-08-19
  • [EN] 4,5-DIHYDRO-ISOXAZOLE DERIVATIVES AND THEIR PHARMACEUTICAL USE<br/>[FR] DERIVES DE 4-5-DIHYDRO-ISOXAZOLE ET LEUR UTILISATION PHARMACEUTIQUE
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:WO2000021959A1
    公开(公告)日:2000-04-20
    The present invention is concerned with the compounds of formula (I), wherein m, n and p are each independently 0 or 1 and q is 0, 1, 2, 3, 4 or 5; A?1=A2 A3=A4¿ is pyridinylidene, pyridazinylidene, pyrimidinylidene, pyrazinylidene or phenylidene; B represents an amide, ketone or oxadiazole; D represents Ar or Het; Q represents a covalent direct bond or a ketone, -N-, -O-, -CR5R6-, amide, ethenyl, imine, sulfonyl, sulfinyl, 3-oxobutenyl, pyrazole isoxazole or thiazole; L represents Ar or Het; R1 represents hydrogen, halo, hydroxy C¿(2-6)?alkenyl, C(2-6)alkynyl, C(3-6)cycloalkyl, C(3-6)cycloalkenyl, cyano, guanidine, nitro NR?17R18¿, an optionally substituted C¿(1-6)?alkyl or C(1-6)alkyloxy; R?2 and R3¿ each independently represent hydrogen, halo, C¿(1-6)?alkyloxy or an optionally substituted C(1-6)alkyl; R?5 and R6¿ each independently represent hydrogen, hydroxy, halo, an optionally substituted C¿(1-6)?alkyl, C(2-6)alkenyl, C(2-6)alkynyl, C(3-6)cycloaklyl, C(3-6)cycloalkenyl, C(1-6)alkyloxy, cyano, (C=O)R?25¿, (C=O)OR16, (SO2)R16, aminocarbonyloxy, amino C¿(1-6)?alkyl, NR?17R18, N¿3, Ar or Het; or R?5 and R6¿ together with the carbon atom to which they are attached, form an Ar or Het; Ar represents an optionally substituted C¿(6-14)?aryl; Het represents an optionally substituted C(1-14)heterocycle; or a N-oxide, pharmaceutically acceptable addition salt, quaternary amine or stereochemically isomeric form thereof; the process for their preparation and compositions comprising them. It further relates to their use as a medicine.
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