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N-methyl-N-propionylbenzamide | 159326-91-7

中文名称
——
中文别名
——
英文名称
N-methyl-N-propionylbenzamide
英文别名
N-methyl-N-propanoylbenzamide
N-methyl-N-propionylbenzamide化学式
CAS
159326-91-7
化学式
C11H13NO2
mdl
——
分子量
191.23
InChiKey
IOTVZZNYJRYPLM-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:
    317.4±15.0 °C(Predicted)
  • 密度:
    1.093±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    37.4
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:6ccfd01c8e07da6499130109e5203d6a
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反应信息

  • 作为产物:
    描述:
    N-甲基苯甲酰胺硫代丙酸S-乙酯N-溴代丁二酰亚胺(NBS) 、 iron(II) chloride 作用下, 以 乙腈 为溶剂, 反应 21.02h, 以48%的产率得到N-methyl-N-propionylbenzamide
    参考文献:
    名称:
    高效氯化铁(II)/ N-溴代琥珀酰亚胺介导的酰亚胺和酰基磺酰胺的合成
    摘要:
    我们已经开发了一种通用且高效的氯化铁(II)/ N-溴琥珀酰亚胺(NBS)介导的方法,该方法通过硫代酯与羧酰胺/磺酰胺的偶联来合成酰亚胺和酰磺酰胺,该方法简单,经济且具有实际优势。
    DOI:
    10.1002/adsc.200800668
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文献信息

  • Amine derivative
    申请人:Ishihara Yuji
    公开号:US20060128690A1
    公开(公告)日:2006-06-15
    The present invention provides a compound represented by the formula wherein Ar 1 is a cyclic group optionally having substituent(s); R is a hydrogen atom, an optionally halogenated C 1-6 alkyl, a phenyl optionally having substituent(s) or a pyridyl optionally having substituent(s); Ra 1 , Ra 2 , Ra 3 and Ra 4 are the same or different and each is a hydrogen atom, an optionally halogenated C 1-6 alkyl or the like; Ar is a monocyclic aromatic ring optionally having substituent(s); Y is an optionally halogenated alkylene group; and R 1 and R 2 are (1) the same or different and each is a hydrogen atom or a C 1-6 alkyl, (2) R 1 and R 2 form a nitrogen-containing heterocycle optionally having substituent(s) together with the adjacent nitrogen atom, or (3) R 1 and Y form a nitrogen-containing heterocycle optionally having substituent(s) together with the adjacent nitrogen atom, and R 2 is a hydrogen atom or a C 1-6 alkyl; provided that when the nitrogen-containing heterocycle formed by R 1 and R 2 together with the adjacent nitrogen atom is a piperazine, or when R is a C 1-4 alkyl, Ar 1 is a cyclic group having substituent(s), or a salt thereof, having a melanin-concentrating hormone antagonistic action and useful as an agent for the prophylaxis or treatment of obesity and the like.
    本发明提供了一种化合物,其表示为式子: 其中,Ar1是一个环状基团,可以具有取代基;R是氢原子,可选卤代的C1-6烷基,苯环,可以具有取代基,或者吡啶环,可以具有取代基;Ra1,Ra2,Ra3和Ra4相同或不同,每个都是氢原子,可选卤代的C1-6烷基或类似物;Ar是一个单环芳香环,可以具有取代基;Y是可选卤代的脂肪族烷基;R1和R2是(1)相同或不同,每个都是氢原子或C1-6烷基,(2)R1和R2与相邻的氮原子一起形成含氮杂环,可以具有取代基,或(3)R1和Y与相邻的氮原子一起形成含氮杂环,可以具有取代基,并且R2是氢原子或C1-6烷基;但是当R1和R2与相邻的氮原子一起形成哌嗪环,或当R是C1-4烷基,Ar1是具有取代基的环状基团或其盐时,该化合物具有黑色素浓集激素拮抗作用,可用作预防或治疗肥胖症等药物。
  • Quinoline compound
    申请人:Ishihara Yuji
    公开号:US20050209213A1
    公开(公告)日:2005-09-22
    A compound, which has a melanin-concentrating hormone antagonistic action and useful as an agent for preventing or treating obesity, and which is represented by the formula: wherein Ar is a cyclic group optionally having substituent(s); X is a bond or a spacer having a main chain of 1 to 6 atoms; R 1 and R 2 are the same or different and each is a hydrogen atom or a hydrocarbon group optionally having substituent(s), or R 1 and R 2 may form, together with the adjacent nitrogen atom, a nitrogen-containing heterocycle optionally having substituent(s); Y is a divalent hydrocarbon group optionally having substituent(s) (except CO); R 3 is a hydrogen atom or a hydrocarbon group optionally having substituent(s); and ring A and ring B may further have substituents, and when ring B further has a substituent, the substituent may be linked to R 1 to form a ring, or a salt thereof, or a prodrug thereof, is provided.
    一种化合物,具有黑色素浓缩激素拮抗作用,可用作预防或治疗肥胖症的药物,其化学式为:其中,Ar是一个环状基团,可以有取代基;X是1到6个原子的主链的键或空隙;R1和R2相同或不同,分别是氢原子或烃基,可以有取代基,或者R1和R2可以与相邻的氮原子一起形成含氮杂环,可以有取代基;Y是一个双价的烃基,可以有取代基(除CO);R3是氢原子或烃基,可以有取代基;环A和环B还可以有取代基,当环B还有取代基时,取代基可以与R1连接形成一个环,或其盐,或其前药。
  • QUINOLINE COMPOUND
    申请人:Takeda Chemical Industries, Ltd.
    公开号:EP1447402A1
    公开(公告)日:2004-08-18
    A compound, which has a melanin-concentrating hormone antagonistic action and useful as an agent for preventing or treating obesity, and which is represented by the formula:    wherein Aris a cyclic group optionally having substituent(s) ; Xis a bond or a spacer having a main chain of 1 to 6 atoms; R1 and R2are the same or different and each is a hydrogen atom or a hydrocarbon group optionally having substituent(s), or R1 and R2 may form, together with the adjacent nitrogen atom, a nitrogen-containing heterocycle optionally having substituent(s); Yis a divalent hydrocarbon group optionally having substituent(s) (except CO); R3is a hydrogen atom or a hydrocarbon group optionally having substituent(s); and ring A and ring Bmay further have substituents, and when ring B further has a substituent, the substituent may be linked to R1 to form a ring, or a salt thereof, or a prodrug thereof, is provided.
    一种化合物,具有拮抗黑色素浓缩激素的作用,可作为预防或治疗肥胖症的药物,由式表示: 式中 Ar 是一个环状基团,可选择具有取代基; X 是主链为 1 至 6 个原子的键或间隔物; R1 和 R2 相同或不同,各自为氢原子或任选具有取代基的烃基,或 R1 和 R2 可与邻近的氮原子一起形成任选具有取代基的含氮杂环; Y 是可选具有取代基的二价烃基(CO 除外); R3 是氢原子或可选具有取代基的烃基;以及 环 A 和环 B 可进一步具有取代基,当环 B 进一步具有取代基时,该取代基可与 R1 连接形成一个环、 或其盐或其原药。
  • AMINE DERIVATIVE
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP1593667A1
    公开(公告)日:2005-11-09
    The present invention provides a compound represented by the formula wherein Ar1 is a cyclic group optionally having substituent(s); R is a hydrogen atom, an optionally halogenated C1-6 alkyl, a phenyl optionally having substituent(s) or a pyridyl optionally having substituent(s); Ra1, Ra2, Ra3 and Ra4 are the same or different and each is a hydrogen atom, an optionally halogenated C1-6 alkyl or the like; Ar is a monocyclic aromatic ring optionally having substituent(s); Y is an optionally halogenated alkylene group; and R1 and R2 are (1) the same or different and each is a hydrogen atom or a C1-6 alkyl, (2) R1 and R2 form a nitrogen-containing heterocycle optionally having substituent(s) together with the adjacent nitrogen atom, or (3) R1 and Y form a nitrogen-containing heterocycle optionally having substituent(s) together with the adjacent nitrogen atom, and R2 is a hydrogen atom or a C1-6 alkyl; provided that when the nitrogen-containing heterocycle formed by R1 and R2 together with the adjacent nitrogen atom is a piperazine, or when R is a C1-4 alkyl, Ar1 is a cyclic group having substituent(s), or a salt thereof, having a melanin-concentrating hormone antagonistic action and useful as an agent for the prophylaxis or treatment of obesity and the like.
    本发明提供了一种由式表示的化合物 其中 Ar1 是任选具有取代基的环状基团; R 是氢原子、任选卤化的 C1-6 烷基、任选具有取代基的苯基或任选具有取代基的吡啶基; Ra1、Ra2、Ra3 和 Ra4 相同或不同,各自为氢原子、任选卤代的 C1-6 烷基或类似物; Ar 是单环芳香环,可选择具有取代基; Y 是任选卤代亚烷基;以及 R1 和 R2 (1) 相同或不同,且各自为氢原子或 C1-6 烷基;(2) R1 和 R2 组成含氮杂环,可选择与相邻氮原子一起具有取代基;或 (3) R1 和 Y 组成含氮杂环,可选择与相邻氮原子一起具有取代基,且 R2 为氢原子或 C1-6 烷基; 条件是当 R1 和 R2 与相邻氮原子一起形成的含氮杂环是哌嗪时,或当 R 是 C1-4 烷基时,Ar1 是具有取代基的环状基团或其盐,具有黑色素浓缩激素拮抗作用,可用作预防或治疗肥胖症等的药物。
  • Spiro compound and organic light-emitting element comprising same
    申请人:LG Chem, Ltd.
    公开号:US11050026B2
    公开(公告)日:2021-06-29
    The present specification provides a compound having a spiro structure and an organic light emitting device including the same.
    本说明书提供了一种具有螺环结构的化合物和一种包含该化合物的有机发光器件。
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