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(+)-2,3-dibromobicyclo<3.2.0>heptan-6-one | 57260-94-3

中文名称
——
中文别名
——
英文名称
(+)-2,3-dibromobicyclo<3.2.0>heptan-6-one
英文别名
(1R,2S,3S,5R)-2,3-dibromo-bicyclo[3.2.0]heptan-6-one;(1R,2S,3S,5R)-2,3-dibromobicyclo[3.2.0]heptan-6-one
(+)-2,3-dibromobicyclo<3.2.0>heptan-6-one化学式
CAS
57260-94-3
化学式
C7H8Br2O
mdl
——
分子量
267.948
InChiKey
SFRZJWGIBHXZBV-CXXDYQFHSA-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):
    1.8
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

点击查看最新优质反应信息

文献信息

  • BICYCLO[2.2.1]HEPT-7-YLAMINE DERIVATIVES AND THEIR USES
    申请人:Finch Harry
    公开号:US20110319446A1
    公开(公告)日:2011-12-29
    Compounds of formula (I) have muscarinic M3 receptor modulating activity; wherein A is an oxygen atom or group —N(R 12 )—; (i) R 1 is C 1 -C 6 -alkyl or a hydrogen atom; and R 2 is a hydrogen atom or a group —R 5 , —Z—Y—R 5 , —Z—NR 9 R 10 ; —Z—CO—NR 9 R 10 ; —Z—NR 9 —CO—R 5 ; or —Z—CO 2 H; and R 3 is a lone pair, or C 1 -C 6 -alkyl in which case the nitrogen atom to which it is attached is a quaternary nitrogen and carries a positive charge; or (ii) R 1 and R 3 together with the nitrogen to which they are attached form a heterocycloalkyl ring, and R 2 is a hydrogen atom; or a group —R 5 , —Z—Y—R 5 , —Z—NR 9 R 10 , —Z—CO—NR 9 R 10 , —Z—NR 9 —CO—R 5 , or —Z—CO 2 H, in which cases the nitrogen atom to which it is attached is a quaternary nitrogen and carries a positive charge; or (iii) R 1 and R 2 together with the nitrogen to which they are attached form a heterocycloalkyl ring, said ring being substituted by a group —Y—R 5 , —Z—Y—R 5 , —Z—NR 9 R 10 ; —Z—CO—NR 9 R 10 ; —Z—NR 9 —CO—R 5 ; or —Z—CO 2 H and R 3 is a lone pair, or C 1 -C 6 -alkyl in which case the nitrogen atom to which it is attached is a quaternary nitrogen and carries a positive charge; R 4 is a group of formula (a), (b), (c) or (d); is an C 1 -C 6 -alkyl, aryl, aryl-fused-cycloalkyl, aryl-fused-heterocycloalkyl, heteroaryl, aryl(C 1 -C 8 -alkyl)-, heteroaryl(C 1 -C 8 -alkyl)-, cycloalkyl or heterocycloalkyl group, and the remaining variables are as defined in the specification.
    式(I)的化合物具有肌动蛋白M3受体调节活性;其中A是氧原子或基团—N(R12)—;(i) R1是C1-C6烷基或氢原子;R2是氢原子或基团—R5、—Z—Y—R5、—Z—NR9R10、—Z—CO—NR9R10、—Z—NR9—CO—R5或—Z—CO2H;R3是孤对电子,或C1-C6烷基,此时它所连接的氮原子是季铵氮并带正电荷;或(ii) R1和R3与它们所连接的氮共同形成杂环烷基环,R2是氢原子;或基团—R5、—Z—Y—R5、—Z—NR9R10、—Z—CO—NR9R10、—Z—NR9—CO—R5或—Z—CO2H,此时它所连接的氮原子是季铵氮并带正电荷;或(iii) R1和R2与它们所连接的氮共同形成杂环烷基环,所述环被基团—Y—R5、—Z—Y—R5、—Z—NR9R10、—Z—CO—NR9R10、—Z—NR9—CO—R5或—Z—CO2H取代,R3是孤对电子,或C1-C6烷基,此时它所连接的氮原子是季铵氮并带正电荷;R4是式(a)、(b)、(c)或(d)的基团;是C1-C6烷基、芳基、芳基螺环烷基、芳基螺杂环烷基、杂芳基、芳基(C1-C8烷基)-、杂芳基(C1-C8烷基)-、环烷基或杂环烷基基团,其余变量如规范所定义。
  • Cyclic Amine Derivatives and Their Uses
    申请人:Finch Harry
    公开号:US20090182033A1
    公开(公告)日:2009-07-16
    Compounds of formula (I) have muscarinic M3 receptor modulating activity; formula (I) wherein R 1 is C 1 -C 6 -alkyl or a hydrogen atom; and R 2 is a hydrogen atom or a group -R 5 or a group, -Z-Y—R 5 , or a group -Z-NR 9 R 10 , or a group -Z-N(R 9 )C(O)R 11 ; and R 3 is a lone pair, or C 1 -C 6 -alkyl; R 4 is selected from one of the groups of formula (a), (b), (c) or (d); formulae (a), (b), (c), (d), Z is a C 1 -C 16 -alkylene, C 2 -C 16 -alkenylene or C 2 -C 16 -alkynylene group; Y is a bond or oxygen atom; R 5 is an C 1 -C 6 -alkyl, aryl, arylalkyl; aryl-fused-cycloalkyl, aryl-fused-heterocycloalkyl, heteroaryl, aryl(C 1 -C 8 -alkyl)-, heteroaryl(C 1 -C 8 -alkyl)-, cycloalkyl or heterocycloalkyl group; R 6 is C 1 -C 6 -alkyl or a hydrogen atom; R 7a and R 7b area C 1 -C 6 -alkyl group or halogen; n and m are independently 0, 1, 2 or 3; R 8a and R 8b are independently selected from the group consisting of aryl, aryl-fused-heterocycloalkyl, heteroaryl, C 1 -C 6 -alkyl, cycloalkyl and hydrogen; R 8c is —OH, C 1 -C 6 -alkyl, hydroxy-C 1 -C 6 -alkyl, or a hydrogen atom; R 8d is C 1 -C 6 -alkyl or a hydrogen atom; R 9 and R 10 are independently a hydrogen atom, C 1 -C 6 -alkyl, aryl aryl-fused-heterocycloalkyl, aryl-fused-cycloalkyl, heteroaryl, aryl(C 1 -C 6 -alkyl)-, or heteroaryl(C 1 -C 6 -alkyl)-group; or R 9 and R 10 together with the nitrogen atom to which they are attached form a heterocyclic ring of 4-8 atoms, optionally containing a further nitrogen or oxygen atom; R 11 is C 1 -C 6 -alkyl or a hydrogen atom; Ar 1 is aryl, heteroaryl or cycloalkyl; Ar 2 are independently aryl, heteroaryl or cycloalkyl; and Q is an oxygen atom, —CH 2 —, —CH 2 CH 2 — or a bond.
    式(I)的化合物具有肌动蛋白M3受体调节活性;其中R1为C1-C6烷基或氢原子;R2为氢原子或基团-R5或基团-Z-Y-R5或基团-Z-NR9R10或基团-Z-N(R9)C(O)R11;R3为孤对电子或C1-C6烷基;R4选自式(a)、(b)、(c)或(d)的一种;式(a)、(b)、(c)、(d)中,Z为C1-C16烷基、C2-C16烯基或C2-C16炔基;Y为键或氧原子;R5为C1-C6烷基、芳基、芳基烷基、芳基-螺环烷基、芳基-杂环螺环烷基、杂芳基、芳基(C1-C8烷基)-、杂芳基(C1-C8烷基)-、环烷基或杂环烷基;R6为C1-C6烷基或氢原子;R7a和R7b为C1-C6烷基或卤素;n和m独立地为0、1、2或3;R8a和R8b独立地选自芳基、芳基-杂环螺环烷基、杂芳基、C1-C6烷基、环烷基和氢;R8c为-OH、C1-C6烷基、羟基-C1-C6烷基或氢原子;R8d为C1-C6烷基或氢原子;R9和R10独立地为氢原子、C1-C6烷基、芳基、芳基-杂环螺环烷基、芳基-螺环烷基、杂芳基、芳基(C1-C6烷基)-或杂芳基(C1-C6烷基)-基团;或R9和R10与它们所连接的氮原子一起形成4-8个原子的杂环,可选地含有进一步的氮或氧原子;R11为C1-C6烷基或氢原子;Ar1为芳基、杂芳基或环烷基;Ar2独立地为芳基、杂芳基或环烷基;Q为氧原子、-CH2-、-CH2CH2-或键。
  • LEE T. V.; ROBERTS S. M.; NEWTON R. F., J. CHEM. SOC. PERKIN TRANS, 1978, PART 1, NO 10, 1189-1182
    作者:LEE T. V.、 ROBERTS S. M.、 NEWTON R. F.
    DOI:——
    日期:——
  • LUH, TIEN-YAU;CHOW, HAK-FUN;LEUNG, WAI, YEE;TAM, SHANG, WAI, TETRAHEDRON, 1985, 41, N 3, 519-525
    作者:LUH, TIEN-YAU、CHOW, HAK-FUN、LEUNG, WAI, YEE、TAM, SHANG, WAI
    DOI:——
    日期:——
  • [EN] BICYCLOR [2.2.1] HEPT-7-YLAMINE DERIVATIVES AND THEIR USE IN THE TREATMENT OF DISEASES AND CONDITIONS IN WHICH M3 MUSCARINIC RECEPTOR ACTIVITY AND BETA-ADRENERGIC ACTIVITY ARE IMPLICATED<br/>[FR] DÉRIVÉS DE BICYCLOR [2.2.1] HEPT-7-YLAMINE ET LEUR UTILISATION DANS LE TRAITEMENT DE MALADIES ET D'ÉTATS PATHOLOGIQUES DANS LESQUELS EST IMPLIQUÉE L'ACTIVITÉ DES RÉCEPTEURS MUSCARINIQUE M3 ET BÊTA-ADRÉNERGIQUE
    申请人:ARGENTA DISCOVERY LTD
    公开号:WO2008149110A1
    公开(公告)日:2008-12-11
    [EN] The present invention relates to compounds of formula (I) having muscarinic M3 receptor and ß-adrenergic receptor modulating activity; wherein R1, R2, R3 and X are as defined herein.
    [FR] La présente invention concerne des composés de formule (I) qui exercent une activité modulante vis à vis des récepteurs muscarinique M3 et ß-adrénergique; R1, R2, R3 et X sont tels que définis ici.
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