2-(4-chlorophenyl)propan-2-amine hydrochloride | 151946-41-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-(4-chlorophenyl)propan-2-amine hydrochloride
• 英文别名: 2-(4-chlorophenyl)propan-2-amine;hydrochloride
• CAS: 151946-41-7
• 化学式: C₉H₁₂ClN*ClH
• mdl: MFCD11855811
• 分子量: 206.115
• InChiKey: QMHIYOHACPZOAB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.333
• 拓扑面积：
  26
• 氢给体数：
  2
• 氢受体数：
  1

安全信息

• 危险性防范说明：
  P261,P280,P301+P312,P302+P352,P305+P351+P338
• 危险性描述：
  H302,H315,H319,H335

反应信息

• 作为反应物：
  描述：

  2-(4-chlorophenyl)propan-2-amine hydrochloride 、 5-氯代戊酰氯 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 5-chloro-N-[1-(4-chlorophenyl)-1-methylethyl]pentanamide
  参考文献：
  名称：

  Therapeutic agents useful for treating inflammatory diseases

  摘要：

  这项发明涉及公式I的化合物及其药学上可接受的盐##STR1##其中R.sub.1、R.sub.2和R.sub.3独立地代表氢、卤素、烷基、烷氧基、苯氧基、苯基、烷氧羰基、--NR.sub.13 R.sub.14、卤代烷氧基、卤代烷基、苄氧基、羟基、羟基烷基、(C.sub.2-6烷氧羰基)乙烯基、--S(O).sub.n R.sub.7、氨基甲酰基烷基、烷氧羰基烷基、--CONR.sub.11 R.sub.12，或者R.sub.1和R.sub.2与苯环一起代表萘基；R.sub.4和R.sub.5独立地代表氢、烷基、苯基或者与碳原子一起代表C.sub.3-6环烷基；R.sub.6代表氢、烷基或.ω.-羟基烷基；A代表C.sub.2-9烷基；R.sub.8代表氢、烷基、卤素、烷氧基、羟基烷基、苄基或苯基；R.sub.9和R.sub.10独立地代表氢、烷基、卤素、烷氧基、苯基、羟基烷基、烷氧羰基、硝基、--NR.sub.30 R.sub.31、烷酰氧基烷基，或氨甲基；这些化合物是抗炎和抗过敏剂。还公开了含有这些化合物的组合物和制备它们的方法。

  公开号：

  US05547972A1

文献信息

• [EN] N-HETEROARYLALKYL-2-(HETEROCYCLYL AND HETEROCYCLYLMETHYL) ACETAMIDE DERIVATIVES AS SSTR4 AGONISTS<br/>[FR] DÉRIVÉS DE N-HÉTÉROARYLALKYLE-2-(HÉTÉROCYCLYLE ET HÉTÉROCYCLYLMÉTHYLE) ACÉTAMIDE UTILISÉS EN TANT QU'AGONISTES DE SSTR4
  申请人：TAKEDA PHARMACEUTICALS CO

  公开号：WO2021202781A1

  公开（公告）日：2021-10-07

  Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein L, n, R1, R2, R6, R7, R8, R9, R10, X3, X4 and X5 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, to pharmaceutical compositions which contain them, and to their use for treating diseases, disorders, and conditions associated with SSTR4.

  揭示了Formula 1的化合物及其药用盐，其中L、n、R1、R2、R6、R7、R8、R9、R10、X3、X4和X5在说明书中有定义。本公开还涉及制备Formula 1化合物的材料和方法，包含它们的药物组合物，以及它们用于治疗与SSTR4相关的疾病、疾患和症状的用途。
• HETEROCYCLIC COMPOUND
  申请人：Takeda Pharmaceutical Company Limited

  公开号：US20210087186A1

  公开（公告）日：2021-03-25

  The present invention provides a compound having a glucosylceramide lowering action (e.g., promoting glucosylceramide metabolism, inhibition of glucosylceramide synthesis, promoting glucosylceramide catabolism, etc.), which is expected to be useful as an agent for the prophylaxis or treatment of lysosome diseases (e.g., Gaucher's disease), neurodegenerative diseases (e.g., Parkinson's disease, Lewy body dementia, multiple-system atrophy) and the like. The present invention relates to a compound represented by the formula (I) wherein each symbol is as described in the specification, or a salt thereof.

  本发明提供一种具有降低葡糖鞘脂的作用（例如促进葡糖鞘脂代谢、抑制葡糖鞘脂合成、促进葡糖鞘脂分解等）的化合物，预计可用作预防或治疗溶酶体疾病（例如高雪氏病）、神经退行性疾病（例如帕金森病、路易体痴呆症、多系统萎缩症）等的药剂。本发明涉及一种由式（I）表示的化合物 其中每个符号如说明书中所述，或其盐。
• Imidazole derivatives as therapeutic agents
  申请人：KNOLL Aktiengesellschaft

  公开号：US05780642A1

  公开（公告）日：1998-07-14

  Compounds of the formula I ##STR1## and pharmaceutically acceptable salts thereof in which R.sub.1 represents hydrogen, halo, cyano, cyanoalkyl, alkyl, alkoxy, phenoxy, phenyl, alkoxycarbonyl, --NR.sub.13 R.sub.14, --N(R.sub.15)SO.sub.2 R16, halogenated alkoxy, halogenated alkyl, arylalkoxy, hydroxy, phenylalkyl, alkoxycarbonylvinyl, --S(O).sub.n R.sub.7, alkoxycarbonylalkyl, carboxyalkyl, --CONR.sub.11 R.sub.12 carbamoylvinyl, --OSO.sub.2 R.sub.21, 4,5-dihydrothiazol-2-yl, 4,4-dimethyl-2-oxazolin-2-yl or --NR.sub.60 R.sub.61 ; or R.sub.1 represents a group of formula --(O).sub.z --L.sub.3 G wherein z equals 0 or 1, L.sub.3 represents a C.sub.1-4 alkylene chain, G represents a group of formula a), b), c), or d): a) --NR.sub.22 R.sub.23 ; b) --S(O).sub.m R.sub.26 ; c) CONR.sub.27 R.sub.28 ; d) --OR.sub.29 ; R.sub.2 and R.sub.3 independently represent hydrogen, halo, alkyl, alkoxy, --NR.sub.13 R.sub.14, halogenated alkoxy, halogenated alkyl, hydroxy, --S(O).sub.n R.sub.7 or --NR.sub.60 R.sub.61 ; L.sub.1 represents e) a bond, or f) alkylene, cycloalkylene or cycloalkylidene; T represents a bond or O, S, SO, SO.sub.2, a carbonyl group, or 1,3-dioxolan-2-ylidene; L.sub.2 represents alkylene, cycloalkylene, or cycloalkylidene; R.sub.6 represents hydrogen or alkyl (optionally substituted by alkoxycarbonyl or hydroxy); Q represents a C.sub.1-9 alkylene chain (optionally substituted by alkyl or hydroxy); and Y represents an optionally substituted imidazole ring; which are antiinflammatory, antiallergic and immunodulant agents. Compositions containing these compounds and processes to make them are also disclosed.

  公式I的化合物及其药学上可接受的盐，其中R.sub.1代表氢、卤素、氰基、氰基烷基、烷基、烷氧基、苯氧基、苯基、烷氧羰基、--NR.sub.13 R.sub.14、--N(R.sub.15)SO.sub.2 R16、卤代烷氧基、卤代烷基、芳基烷氧基、羟基、苯基烷基、烷氧羰基乙烯基、--S(O).sub.n R.sub.7、烷氧羰基烷基、羧基烷基、--CONR.sub.11 R.sub.12 氨基乙烯基、--OSO.sub.2 R.sub.21、4,5-二氢噻唑-2-基、4,4-二甲基-2-噁唑-2-基或--NR.sub.60 R.sub.61；或R.sub.1代表公式--(O).sub.z --L.sub.3 G中的一个基团，其中z等于0或1，L.sub.3代表C.sub.1-4烷基链，G代表公式a)、b)、c)或d)中的一个基团：a) --NR.sub.22 R.sub.23；b) --S(O).sub.m R.sub.26；c) CONR.sub.27 R.sub.28；d) --OR.sub.29；R.sub.2和R.sub.3独立地代表氢、卤素、烷基、烷氧基、--NR.sub.13 R.sub.14、卤代烷氧基、卤代烷基、羟基、--S(O).sub.n R.sub.7或--NR.sub.60 R.sub.61；L.sub.1代表e)键，或f)烷基、环烷基或环烷基亚甲基；T代表键或O、S、SO、SO.sub.2、羰基，或1,3-二氧杂环戊二烯基；L.sub.2代表烷基、环烷基或环烷基亚甲基；R.sub.6代表氢或烷基（可选地被烷氧羰基或羟基取代）；Q代表C.sub.1-9烷基链（可选地被烷基或羟基取代）；Y代表一个可选取代的咪唑环；这些化合物是抗炎、抗过敏和免疫调节剂。还公开了含有这些化合物的组合物和制备它们的方法。
• Phenoxy-, phenylthio-, benzoyl-alkyleneaminoalkylene-imidazole
  申请人：Knoll Aktiengesellschaft

  公开号：US06031109A1

  公开（公告）日：2000-02-29

  Compounds of formula I ##STR1## where R.sub.1 -R.sub.3, L.sub.1, T, L.sub.2 --N--Q--Y and R.sub.6 are as defined in the specification, and pharmaceutically acceptable salts thereof which are antiinflammatory, antiallergic and immunomodulant agents, compositions containing these compounds and processes to make them.

  式子I的化合物，其中R.sub.1-R.sub.3，L.sub.1，T，L.sub.2--N--Q--Y和R.sub.6的定义如说明书中所述，并且其药学上可接受的盐是抗炎，抗过敏和免疫调节剂，包含这些化合物的组合物以及制造它们的过程。
• Imidazole derivatives for blocking the release of arachidonic acid from phospholipids
  申请人：Abbott Laboratories

  公开号：US06326500B1

  公开（公告）日：2001-12-04

  Compounds of formula (I) and salts thereof, wherein R1 is hydrogen, halo, cyano, cyanoalkyl, alkyl, alkoxy, phenoxy, phenyl, alkoxycarbonyl, —NR13R14, —N(R15)SO2R16, haloalkoxy, haloalkyl, arylalkoxy, hydroxy, phenylalkyl, alkoxycarbonylvinyl, —SOnR7, alkoxycarbonylalkyl, carboxylalkyl, —CONR11R12, carbamoylvinyl, —O—SO2R21, 4,5-dihydrothiazol-2-yl, 4,4-dimethyl-2-oxazolin-2-yl, —NR60R61 or —(O)z—L3—G (G=−NR22R23, —SOmR26, CONR27R28 or —OR29); R2 and R3 are independently hydrogen halo, alkyl, alkoxy, —NR13R14, haloalkoxy, haloalkyl, hydroxy, —SOnR7 or —NR60R61; L1 is a bond, alkylene, cycloalkylene or cycloalkylidene; T is a bond, O, S, SO, SO2, CO or 1,3-dioxolan-2-ylidene; L2 is alkylene, cycloalkylene or cycloalkylidene; R6 is hydrogen or alkyl; Q is alkylene; and Y is imidazolyl, which are antiinflammatory, antiallergic and immunodulant agents. Compositions containing these compounds and processes to make them are also disclosed.

  化合物式（I）及其盐，其中R1为氢，卤，氰，氰基烷基，烷基，烷氧基，苯氧基，苯基，烷氧羰基，-NR13R14，-N（R15）SO2R16，卤代烷氧基，卤代烷基，芳基烷氧基，羟基，苯基烷基，烷氧羰基乙烯基，-SOnR7，烷氧羰基烷基，羧基烷基，-CONR11R12，氨基乙烯基，-O-SO2R21，4,5-二氢噻唑-2-基，4,4-二甲基-2-噁唑烷-2-基，-NR60R61或-(O)z-L3-G（G= -NR22R23，-SOmR26，CONR27R28或-OR29）;R2和R3独立地为氢，卤，烷基，烷氧基，-NR13R14，卤代烷氧基，卤代烷基，羟基，-SOnR7或-NR60R61;L1为键，烷基，环烷基或环烷基亚甲基;T为键，O，S，SO，SO2，CO或1,3-二氧杂环戊烷-2-基亚甲基;L2为烷基，环烷基或环烷基亚甲基;R6为氢或烷基;Q为烷基;Y为咪唑基，具有抗炎，抗过敏和免疫调节作用。还公开了含有这些化合物的组合物和制备它们的过程。