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4-Aza-dibenzcyclohepten | 4940-69-6

中文名称
——
中文别名
——
英文名称
4-Aza-dibenzcyclohepten
英文别名
11H-benzo[5,6]cyclohepta[1,2-b]pyridine;4-Azatricyclo[9.4.0.03,8]pentadeca-1(15),3(8),4,6,9,11,13-heptaene
4-Aza-dibenz<a,d>cyclohepten化学式
CAS
4940-69-6
化学式
C14H11N
mdl
——
分子量
193.248
InChiKey
VVJQGUSMDLABEG-UHFFFAOYSA-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):
    3.3
  • 重原子数:
    15
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    12.9
  • 氢给体数:
    0
  • 氢受体数:
    1

文献信息

  • [EN] PROCESS FOR THE PREPARATION OF LORATADINE<br/>[FR] PROCEDE DE PREPARATION DE LORATADINE
    申请人:MOREPEN LAB LTD
    公开号:WO2004080997A1
    公开(公告)日:2004-09-23
    A process for the production of loratadine chemically known as 8-chloro-11-(1-ethoxycarbonyl-4-piperidylidene)-6,11-dihydro-5H-benzo[5,6]cycloheptal[1,2-B]pyridene has been described. The process comprises reacting a tri-cyclic aromatic ketone with an organometallic compound containing Mg in presence of organic solvent then hydrolyzing and isolating loratadine by conventional methods wherein the reaction between cyclic ketone and the said organometallic compound is effected at a glacial temperature.
    已经描述了一种生产洛拉替丁的过程,化学上称为8--11-(1-乙氧羰基-4-哌啶基)-6,11-二氢-5H-苯并[5,6]环庚[1,2-B]吡啶。该过程包括将三环芳香酮与含的有机属化合物在有机溶剂存在下反应,然后通过常规方法解和分离洛拉替丁,其中环酮与所述有机属化合物之间的反应在极低温下进行。
  • Novel benzo [5,6] cyclohepta [1,2-b] pyridine derivatives and antiallergic agents comprising same
    申请人:SS PHARMACEUTICAL CO., LTD.
    公开号:EP0495484A1
    公开(公告)日:1992-07-22
    Benzo[5,6]cyclohepta[1,2-b]pyridine derivatives of the following formula: wherein R¹ represents a cyano, carbamoyl, alkylsulfoxy, alkylsulfonyl, tetrazolyl or sulfonic acid group, and R² represents a hydrogen atom, a cyano, phenyl, aralkyl, alkoxycarbonylalkyl, aminoalkylcarbamoylalkyl or lower alkyl group, or a group or -X-R₄, X being an oxygen or sulfur atom, R³ standing for a hydrogen atom or a substituted or unsubstituted lower alkyl, phenyl or aralkyl group, and R⁴ being a substituted or unsubstituted lower alkyl, phenyl or aralkyl group or an aminoalkyl group, and salts thereof. Antiallergic and antihistamic agents containing one of the above derivatives or salts as an active ingredient are also described.
    以下是Benzo[5,6]cyclohepta[1,2-b]pyridine衍生物化学式:其中R¹代表基,基甲酰基,烷基磺酸氧基,烷基磺酰基,四氮唑基或磺酸基团,R²代表氢原子,基,苯基,芳基烷基,烷氧羰基烷基,基烷基甲酰基烷基或低碳基团,或-X-R₄的基团,其中X代表氧或原子,R³代表氢原子或取代或未取代的低碳基,苯基或芳基烷基团,R⁴代表取代或未取代的低碳基,苯基或芳基烷基团或基烷基团,以及其盐。还描述了含有上述衍生物或盐作为活性成分的抗过敏和抗组胺药物。
  • Cyclooctynes for click chemistry
    申请人:Massachusetts Institute of Technology
    公开号:US11377424B1
    公开(公告)日:2022-07-05
    Provided herein are dibenzocyclooctyne compounds useful as reagents in 1,3-dipolar cycloaddition reactions, and methods for their preparation.
    本文提供了二苯并环辛炔化合物,可用作1,3-二极体环加成反应的试剂,并提供了它们的制备方法。
  • Benzo(5,6)cyclohepta(1,2-B)pyridine derivatives for the inhibition of farnesyl protein transferase
    申请人:SCHERING CORPORATION
    公开号:EP1156046A1
    公开(公告)日:2001-11-21
    Novel compounds, such as formulae (I) and (II), are disclosed. The compounds are useful for inhibiting the abnormal growth of cells, for inhibiting farnesyl protein transferase, and for treating cancers.
    本研究公开了新型化合物,如式(I)和式(II)。这些化合物可用于抑制细胞的异常生长、抑制法尼酰蛋白转移酶和治疗癌症。
  • Fused polycyclic compounds, compositions, methods of manufacture, and their use as PAF antagonists, antihistamines and/or antiinflammatory agents
    申请人:SCHERING CORPORATION
    公开号:EP0339978B1
    公开(公告)日:1996-08-21
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同类化合物

()-2-(5-甲基-2-氧代苯并呋喃-3(2)-亚乙基)乙酸乙酯 (双(2,2,2-三氯乙基)) (乙基N-(1H-吲唑-3-基羰基)ethanehydrazonoate) (Z)-3-[[[2,4-二甲基-3-(乙氧羰基)吡咯-5-基]亚甲基]吲哚-2--2- (S)-(-)-5'-苄氧基苯基卡维地洛 (S)-(-)-2-(α-(叔丁基)甲胺)-1H-苯并咪唑 (S)-(-)-2-(α-甲基甲胺)-1H-苯并咪唑 (S)-氨氯地平-d4 (S)-8-氟苯并二氢吡喃-4-胺 (S)-4-(叔丁基)-2-(喹啉-2-基)-4,5-二氢噁唑 (S)-4-氯-1,2-环氧丁烷 (S)-3-(2-(二氟甲基)吡啶-4-基)-7-氟-3-(3-(嘧啶-5-基)苯基)-3H-异吲哚-1-胺 (S)-2-(环丁基氨基)-N-(3-(3,4-二氢异喹啉-2(1H)-基)-2-羟丙基)异烟酰胺 (SP-4-1)-二氯双(喹啉)-钯 (SP-4-1)-二氯双(1-苯基-1H-咪唑-κN3)-钯 (R,S)-可替宁N-氧化物-甲基-d3 (R,S)-六氢-3H-1,2,3-苯并噻唑-2,2-二氧化物-3-羧酸叔丁酯 (R)-(+)-5'-苄氧基卡维地洛 (R)-(+)-2,2'',6,6''-四甲氧基-4,4''-双(二苯基膦基)-3,3''-联吡啶(1,5-环辛二烯)铑(I)四氟硼酸盐 (R)-卡洛芬 (R)-N'-亚硝基尼古丁 (R)-DRF053二盐酸盐 (R)-4-异丙基-2-恶唑烷硫酮 (R)-3-甲基哌啶盐酸盐; (R)-2-苄基哌啶-1-羧酸叔丁酯 (N-(Boc)-2-吲哚基)二甲基硅烷醇钠 (N-{4-[(6-溴-2-氧代-1,3-苯并恶唑-3(2H)-基)磺酰基]苯基}乙酰胺) (E)-2-氰基-3-(5-(2-辛基-7-(4-(对甲苯基)-1,2,3,3a,4,8b-六氢环戊[b]吲哚-7-基)-2H-苯并[d][1,2,3]三唑-4-基)噻吩-2-基)丙烯酸 (E)-2-氰基-3-[5-(2,5-二氯苯基)呋喃-2-基]-N-喹啉-8-基丙-2-烯酰胺 (8α,9S)-(+)-9-氨基-七氢呋喃-6''-醇,值90% (6R,7R)-7-苯基乙酰胺基-3-[(Z)-2-(4-甲基噻唑-5-基)乙烯基]-3-头孢唑啉-4-羧酸二苯甲基酯 (6-羟基嘧啶-4-基)乙酸 (6,7-二甲氧基-4-(3,4,5-三甲氧基苯基)喹啉) (6,6-二甲基-3-(甲硫基)-1,6-二氢-1,2,4-三嗪-5(2H)-硫酮) (5aS,6R,9S,9aR)-5a,6,7,8,9,9a-六氢-6,11,11-三甲基-2-(2,3,4,5,6-五氟苯基)-6,9-甲基-4H-[1,2,4]三唑[3,4-c][1,4]苯并恶嗪四氟硼酸酯 (5R,Z)-3-(羟基((1R,2S,6S,8aS)-1,3,6-三甲基-2-((E)-prop-1-en-1-yl)-1,2,4a,5,6,7,8,8a-八氢萘-1-基)亚甲基)-5-(羟甲基)-1-甲基吡咯烷-2,4-二酮 (5E)-5-[(2,5-二甲基-1-吡啶-3-基-吡咯-3-基)亚甲基]-2-亚磺酰基-1,3-噻唑烷-4-酮 (5-(4-乙氧基-3-甲基苄基)-1,3-苯并二恶茂) (5-溴-3-吡啶基)[4-(1-吡咯烷基)-1-哌啶基]甲酮 (5-氯-2,1,3-苯并噻二唑-4-基)-氨基甲氨基硫代甲酸甲酯一氢碘 (5-氨基-6-氰基-7-甲基[1,2]噻唑并[4,5-b]吡啶-3-甲酰胺) (5-氨基-1,3,4-噻二唑-2-基)甲醇 (4aS-反式)-八氢-1H-吡咯并[3,4-b]吡啶 (4aS,9bR)-6-溴-2,3,4,4a,5,9b-六氢-1H-吡啶并[4,3-B]吲哚 (4S,4''S)-2,2''-环亚丙基双[4-叔丁基-4,5-二氢恶唑] (4-(4-氯苯基)硫代)-10-甲基-7H-benzimidazo(2,1-A)奔驰(德)isoquinolin-7一 (4-苄基-2-甲基-4-nitrodecahydropyrido〔1,2-a][1,4]二氮杂) (4-甲基环戊-1-烯-1-基)(吗啉-4-基)甲酮 (4-己基-2-甲基-4-nitrodecahydropyrido〔1,2-a][1,4]二氮杂) (4,5-二甲氧基-1,2,3,6-四氢哒嗪)