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2-[(二甲基氨基)甲基]四氢萘-1-酮 | 7353-59-5

中文名称
2-[(二甲基氨基)甲基]四氢萘-1-酮
中文别名
2-((二甲氨基)甲基)-3,4-二氢萘-1(2H)-酮
英文名称
2-dimethylaminomethyl-3,4-dihydro-naphthalen-1-one
英文别名
2-Dimethylaminomethyl-tetralon-(1);2-Dimethylaminomethyltetralone;2-[(dimethylamino)methyl]-3,4-dihydro-2H-naphthalen-1-one
2-[(二甲基氨基)甲基]四氢萘-1-酮化学式
CAS
7353-59-5
化学式
C13H17NO
mdl
——
分子量
203.284
InChiKey
OMCOACHXKJOZMD-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

物化性质

  • 沸点:
    308.0±11.0 °C(Predicted)
  • 密度:
    1.047±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:574d66c673985db52144bc5db62c27e9
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
    • 1
    • 2

反应信息

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文献信息

  • A Modified Mannich Reaction Using 1.3-Dioxolane.
    作者:Kazuharu SUMITA、Masayuki KOUMORI、Sachio OHNO
    DOI:10.1248/cpb.42.1676
    日期:——
    Mannich reaction of ketones using 1, 3-dioxolane instead of formaldehyde, paraformaldehyde, or 1, 3, 5-trioxane afforded the corresponding Mannich bases in high yields. Under the same conditions the aminomethylation of aromatics did not proceed but the intramolecular aminomethylation, like a Pictet-Spengler type reaction, proceeded smoothly.
    使用1,3-二恶烷代替甲醛三聚甲醛1,3,5-三恶烷进行的酮的Mannich反应,以高产率得到了相应的Mannich碱。在同样的条件下,芳香族的胺甲基化反应并未进行,但类似于Pictet-Spengler类型的分子内胺甲基化反应却顺利进行。
  • Amino substituted tetrahydropleiadenes
    申请人:Sandoz, Inc.
    公开号:US03956391A1
    公开(公告)日:1976-05-11
    1,2,3,12a-tetrahydro-1-(substituted-aminomethyl)-7-methylene-7(12H) pleiadenes, e.g., 1,2,3,12a-tetrahydro-1-(dimethylaminomethyl)-7-methylene-7(12H)-pleiadene, prepared by various methods including acid dehydration of the corresponding 1,2,3,12a-tetrahydro-1-(dimethylaminomethyl)-7-methyl-7(12H) -pleiaden-7-ols, are useful as anti-depressants.
    1,2,3,12a-四氢-1-(取代甲基)-7-亚甲基-7(12H)普莱阿丁,例如,1,2,3,12a-四氢-1-(二甲胺甲基)-7-亚甲基-7(12H)-普莱阿丁,通过包括酸脱的各种方法制备,例如对应的1,2,3,12a-四氢-1-(二甲胺甲基)-7-甲基-7(12H)-普莱阿丁-7-醇,可用作抗抑郁药。
  • PROCESS FOR PREPARATION OF NORBORNENE DERIVATIVES
    申请人:JX Nippon Oil & Energy Corporation
    公开号:EP2444386A1
    公开(公告)日:2012-04-25
    A method for producing a norbornene derivative, comprising: a first step of forming a Mannich base by reacting a carbonyl compound and an amine compound with each other in an acidic solvent, to thereby obtain a reaction liquid comprising the Mannich base in the acidic solvent, the acidic solvent comprising a formaldehyde derivative and 0.01 mol/L or more of an acid represented by the formula: HX (In the formula, X represents F or the like), the carbonyl compound being represented by any of the following general formulae (1) to (3): [in formulae (1) to (3), R1, R2, R3, R4, R5, and R6 each independently represent a hydrogen atom or the like, and n represents an integer of any of 0 to 4], the amine compound being represented by the following general formula (4): [in the formula (4), R7S each independently represent a linear chain saturated hydrocarbon group having 1 to 20 carbon atoms or the like, and X- represents F- or the like], the Mannich base being represented by any of the following general formulae (5) to (7): [R1, R2, R3, R4, R5, R6, and n in the formulae (5) to (7) have the same meanings as those of R1, R2, R3, R4, R5, R6, and n in the formulae (1) to (3), and R7 and X- in the formulae (5) to (7) have the same meanings as those of R7 and X- in the formula (4)] and a second step of reacting the Mannich base and a diene compound with each other by adding an organic solvent, a base in an amount of 1.0 to 20.0 equivalents to the acid, and the diene compound to the reaction liquid, and then heating the reaction liquid, to thereby form a norbornene derivative, the diene compound being represented by the following general formula (8): [in the formula (8), R8 represents a hydrogen atom or the like], the norbornene derivative being represented by any of the following general formulae (9) to (11): [R1, R2, R3, R4, R5, R6, and n in the formulae (9) to (11) have the same meanings as those of R1, R2, R3, R4, R5, R6, and n in the formulae (1) to (3), and R8 in the formulae (9) to (11) has the same meaning as that of R8 in the formula (8)].
    一种制备去氢莰烯生物的方法,包括以下步骤:第一步,在酸性溶剂中使羰基化合物和胺基化合物反应,形成曼尼希碱,从而在酸性溶剂中获得包含曼尼希碱的反应液,所述酸性溶剂包括甲醛生物和代表为HX的酸,其中HX中的X代表F或类似物,所述羰基化合物由以下通式(1)至(3)中的任一通式表示:[在通式(1)至(3)中,R1、R2、R3、R4、R5和R6各自独立地代表氢原子或类似物,n代表0至4中的任一整数],所述胺基化合物由以下通式(4)表示:[在通式(4)中,R7S各自独立地代表具有1至20个碳原子或类似物的线性链饱和碳氢基团,X-代表F-或类似物],所述曼尼希碱由以下通式(5)至(7)中的任一通式表示:[在通式(5)至(7)中,R1、R2、R3、R4、R5、R6和n的含义与通式(1)至(3)中的R1、R2、R3、R4、R5、R6和n的含义相同,通式(5)至(7)中的R7和X-的含义与通式(4)中的R7和X-的含义相同];第二步,通过向反应液中加入有机溶剂、相当于酸的1.0至20.0当量的碱和二烯化合物,然后加热反应液,使曼尼希碱与二烯化合物发生反应,从而形成去氢莰烯生物,所述二烯化合物由以下通式(8)表示:[在通式(8)中,R8代表氢原子或类似物],所述去氢莰烯生物由以下通式(9)至(11)中的任一通式表示:[在通式(9)至(11)中,R1、R2、R3、R4、R5、R6和n的含义与通式(1)至(3)中的R1、R2、R3、R4、R5、R6和n的含义相同,通式(9)至(11)中的R8的含义与通式(8)中的R8的含义相同]。
  • A New Entry to the Synthesis of 1,2-Benzenediol Congeners.
    作者:Yutaka OZAKI、Ikumi OSHIO、Yasue OHSUGA、Shouichi KABURAGI、Zhung-Zhu SUNG、Sang-Won KIM
    DOI:10.1248/cpb.39.1132
    日期:——
    1, 2-Benzenediols were synthesized via 1, 1-bis(ethylthio)-3-cyclohexen-2-one derivatives, which were prepared by condensation of 1, 1-bis(ethylthio)-2-propanone with Mannich bases. Regioselective preparation of their monoethers was also achieved.
    1, 2-苯二醇通过1, 1-双(乙基)-3-环己烯-2-酮衍生物合成,这些衍生物是通过1, 1-双(乙基)-2-丙酮与曼尼希碱的缩合反应制备的。同时,单醚的位选择性合成也得以实现。
  • Cyclic substituted aminomethyl compounds and medicaments comprising these compounds
    申请人:——
    公开号:US20030166708A1
    公开(公告)日:2003-09-04
    Cyclic substituted aminomethyl compounds of general formula IA and IB, methods for production thereof, intermediates in said production methods, a medicament containing at least one of said cyclic substituted aminomethyl compounds, the use of said cyclic substituted aminomethyl compounds for the production of a medicament, pharmaceutical compositions containing said compounds, and methods for the treatment of pain, incontinence, pruritis, tinnitus aurium and/or diarrhea using said pharmaceutical compositions.
    一般式IA和IB的环替代甲基化合物,其生产方法,生产方法中的中间体,含有至少一种该环替代甲基化合物的药物,利用该环替代甲基化合物生产药物,含有该化合物的药物组合物,以及使用该药物组合物治疗疼痛、尿失禁、瘙痒、耳鸣和/或腹泻的方法。
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同类化合物

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