1-methylcyclopropyl 4-((1R,2R)-2-((2-fluoro-4-(1H-tetrazol-1-yl)benzyloxy)methyl)cyclopropyl)piperidine-1-carboxylate | 1416365-86-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 1-methylcyclopropyl 4-((1R,2R)-2-((2-fluoro-4-(1H-tetrazol-1-yl)benzyloxy)methyl)cyclopropyl)piperidine-1-carboxylate
• 英文别名: 1-methylcyclopropyl 4-((1R,2R)-2-((2-fluoro-4-(1H-tetrazol-yl)benzvloxy)methyl)cyclopropyl)piperidine-1-carboxylate；(1-methylcyclopropyl) 4-[(1R,2R)-2-[[2-fluoro-4-(tetrazol-1-yl)phenyl]methoxymethyl]cyclopropyl]piperidine-1-carboxylate
• CAS: 1416365-86-0
• 化学式: C₂₂H₂₈FN₅O₃
• 分子量: 429.494
• InChiKey: KWTCVUPNCYCSHK-PKOBYXMFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  31
• 可旋转键数：
  8
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.64
• 拓扑面积：
  82.4
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  4-(3-羟基丙-1-炔-1-基)哌啶-1-甲酸叔丁酯 在 喹啉 、 盐酸 、 tris-(dibenzylideneacetone)dipalladium(0) 、 sodium azide 、 氢气 、 diethylzinc 、 sodium hexamethyldisilazane 、 溶剂黄146 、 三乙胺 、 lithium hexamethyldisilazane 、 2-(二环己基膦基)联苯 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 乙二醇二甲醚 、 二氯甲烷 、 乙酸乙酯 、 乙腈 为溶剂， -20.0~100.0 ℃ 、101.33 kPa 条件下， 反应 6.92h， 生成 1-methylcyclopropyl 4-((1R,2R)-2-((2-fluoro-4-(1H-tetrazol-1-yl)benzyloxy)methyl)cyclopropyl)piperidine-1-carboxylate
  参考文献：
  名称：

  Design of Potent and Orally Active GPR119 Agonists for the Treatment of Type II Diabetes

  摘要：

  We report herein the design and synthesis of a series of potent and selective GPR119 agonists. Our objective was to develop a GPR119 agonist with properties that were suitable for fixed-dose combination with a DPP4 inhibitor. Starting from a phenoxy analogue (1), medicinal chemistry efforts directed toward reducing half-life and increasing solubility led to the synthesis of a series of benzyloxy analogues. Compound 28 was chosen for further profiling because of its favorable physicochemical properties and excellent GPR119 potency across species. This compound exhibited a clean off-target profile in counterscreens and good in vivo efficacy in mouse oGTT.

  DOI：

  10.1021/acsmedchemlett.5b00207

文献信息

• [EN] SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS, AND METHODS OF TREATMENT<br/>[FR] COMPOSÉS CYCLOPROPYLÉS SUBSTITUÉS, COMPOSITIONS CONTENANT DE TELS COMPOSÉS ET PROCÉDÉS DE TRAITEMENT
  申请人：MERCK SHARP & DOHME

  公开号：WO2012173917A1

  公开（公告）日：2012-12-20

  Substituted cyclopropyl compounds of the formula I: and pharmaceutically acceptable salts thereof are disclosed as useful for treating or preventing type 2 diabetes and similar conditions. The compounds are useful as agonists of the G-protein coupled receptor GPR-119. Pharmaceutical compositions and methods of treatment are also included.

  公开了具有以下化学式I的环丙基化合物及其药学上可接受的盐，用于治疗或预防2型糖尿病和类似疾病。这些化合物可用作G蛋白偶联受体GPR-119的激动剂。还包括药物组合物和治疗方法。
• SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS, AND METHODS OF TREATMENT
  申请人：Miller Michael

  公开号：US20140128368A1

  公开（公告）日：2014-05-08

  Substituted cyclopropyl compounds of the formula I: and pharmaceutically acceptable salts thereof are disclosed as useful for treating or preventing type 2 diabetes and similar conditions. The compounds are useful as agonists of the G-protein coupled receptor GPR-119. Pharmaceutical compositions and methods of treatment are also included.

  公开了式I的替代环丙基化合物及其药学上可接受的盐，用于治疗或预防2型糖尿病和类似疾病。这些化合物可用作G蛋白偶联受体GPR-119的激动剂。还包括制药组合物和治疗方法。
• US9006228B2
  申请人：——

  公开号：US9006228B2

  公开（公告）日：2015-04-14
• Design of Potent and Orally Active GPR119 Agonists for the Treatment of Type II Diabetes
  作者：Ping Liu、Zhiyong Hu、Byron G. DuBois、Christopher R. Moyes、David N. Hunter、Cheng Zhu、Nam Fung Kar、Yuping Zhu、Joie Garfunkle、Ling Kang、Gary Chicchi、Anka Ehrhardt、Andrea Woods、Toru Seo、Morgan Woods、Margaret van Heek、Karen H. Dingley、Jianmei Pang、Gino M. Salituro、Joyce Powell、Jenna L. Terebetski、Viktor Hornak、Louis-Charles Campeau、Joe Lamberson、Fez Ujjainwalla、Michael Miller、Andrew Stamford、Harold B. Wood、Timothy Kowalski、Ravi P. Nargund、Scott D. Edmondson

  DOI：10.1021/acsmedchemlett.5b00207

  日期：2015.8.13

  We report herein the design and synthesis of a series of potent and selective GPR119 agonists. Our objective was to develop a GPR119 agonist with properties that were suitable for fixed-dose combination with a DPP4 inhibitor. Starting from a phenoxy analogue (1), medicinal chemistry efforts directed toward reducing half-life and increasing solubility led to the synthesis of a series of benzyloxy analogues. Compound 28 was chosen for further profiling because of its favorable physicochemical properties and excellent GPR119 potency across species. This compound exhibited a clean off-target profile in counterscreens and good in vivo efficacy in mouse oGTT.