2-(1-methoxycarbonyl-ethoxy)benzoic acid methyl ester | 133867-02-4

• 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-(1-methoxycarbonyl-ethoxy)benzoic acid methyl ester
• 英文别名: 2-(1-Methoxycarbonylethoxy)benzoic acid methyl ester；methyl 2-(1-methoxy-1-oxopropan-2-yl)oxybenzoate
• CAS: 133867-02-4
• 化学式: C₁₂H₁₄O₅
• 分子量: 238.24
• InChiKey: PEWYUMXTTSQWTB-UHFFFAOYSA-N

物化性质

• 沸点：
  323.8±17.0 °C(Predicted)
• 密度：
  1.163±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  17
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  61.8
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-(1-methoxycarbonyl-ethoxy)benzoic acid methyl ester 在 potassium carbonate 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 0.17h， 以71%的产率得到2-甲基-3(2H)-苯并呋喃酮
  参考文献：
  名称：

  Hammet Constants Effects in Microwave Cascade Etherification-Cyclization-Krapcho Reaction to Access [2,3]-Dihydrobenzofuran-3-ones from Salicylic Derivatives

  摘要：

  Two methods were evaluated for the synthesis of substituted [2,3]-dihydro-2-methyl-benzofuran-3-ones from corresponding salicylate esters under microwave irradiation. A two-step sequence via ether intermediates was convenient for various substituted salicylate derivatives, while the second strategy involving a one-pot procedure was efficient for electron-donating substituted salicylates. Results allowed correlation of the Hammett constants effects in the intramolecular cyclization of O-ethoxycarbonyl ether of salicylic esters.

  DOI：

  10.1080/00397911.2010.533806
• 作为产物：
  描述：

  2-氯丙酸甲酯 、 水杨酸甲酯 在 potassium carbonate 、 sodium iodide 作用下， 以 丙酮 为溶剂， 反应 48.0h， 以22.4%的产率得到2-(1-methoxycarbonyl-ethoxy)benzoic acid methyl ester
  参考文献：
  名称：

  FUNCTIONALIZED PHENOLIC COMPOUNDS AND POLYMERS THEREFROM

  摘要：

  本发明涉及公式I的化合物，这些化合物是官能化酚类化合物，以及由它们形成的聚合物。从官能化酚类化合物形成的聚合物预计具有可控的降解特性，使它们能够在所需的时间范围内释放活性成分。这些聚合物还预计在各种医疗应用中有用。

  公开号：

  US20090170927A1

文献信息

• Functionalized drugs and polymers derived therefrom
  申请人：Bezwada S. Rao

  公开号：US20060172983A1

  公开（公告）日：2006-08-03

  Compounds selected from: where DRUG-OH, DRUG-COOH and DRUG-NH 2 are biologically active compounds; each X is independently selected from —CH 2 COO— (glycolic acid moiety), —CH(CH 3 )COO— (lactic acid moiety), —CH 2 CH 2 OCH 2 COO— (dioxanone moiety), —CH 2 CH 2 CH 2 CH 2 CH 2 COO— (caprolactone moiety), —(CH 2 ) y COO—, where y is 2-4 or 6-24 and —(CH 2 CH 2 O) z CH 2 COO—, where z is 2-24; each Y is independently selected from —COCH 2 O— (glycolic ester moiety), —COCH(CH 3 )O— (lactic ester moiety), —COCH 2 OCH 2 CH 2 O— (dioxanone ester moiety), —COCH 2 CH 2 CH 2 CH 2 CH 2 O— (caprolactone ester moiety), —CO(CH 2 ) m O—, where m is 2-4 or 6-24 and —COCH 2 O(CH 2 CH 2 O) n — where n is between 2-24; R′ is hydrogen, benzyl or an alkyl group, the alkyl group being either straight-chained or branched; and p is 1-6. Multi-functional compounds and drug dimers, oligomers and polymers are also disclosed.

  从中选择的化合物：其中DRUG-OH，DRUG-COOH和DRUG-NH2是生物活性化合物；每个X独立地从—CH2COO—（乙二酸基团），—CH(CH3)COO—（乳酸基团），—CH2CH2OCH2COO—（二氧杂环己酮基团），—CH2CH2CH2CH2CH2COO—（己内酯基团），—(CH2)yCOO—中选择，其中y为2-4或6-24和—(CH2CH2O)zCH2COO—，其中z为2-24；每个Y独立地从—COCH2O—（乙二酸酯基团），—COCH(CH3)O—（乳酸酯基团），—COCH2OCH2CH2O—（二氧杂环己酮酯基团），—COCH2CH2CH2CH2CH2O—（己内酯酯基团），—CO(CH2)mO—，其中m为2-4或6-24和—COCH2O(CH2CH2O)n—，其中n为2-24；R′为氢，苄基或烷基，烷基可以是直链或支链；p为1-6。还披露了多功能化合物和药物二聚体、寡聚体和聚合物。
• FUNCTIONALIZED DRUGS AND POLYMERS THEREFROM
  申请人：Bezwada Rao S.

  公开号：US20100152272A1

  公开（公告）日：2010-06-17

  Compounds selected from: where DRUG-OH, DRUG-COOH and DRUG-NH 2 are biologically active compounds; each X is independently selected from —CH 2 COO— (glycolic acid moiety), —CH(CH 3 )COO— (lactic acid moiety), —CH 2 CH 2 OCH 2 COO— (dioxanone moiety), —CH 2 CH 2 CH 2 CH 2 CH 2 COO— (caprolactone moiety), —(CH 2 ) y COO—, where y is 2-4 or 6-24 and —(CH 2 CH 2 O) z CH 2 COO—, where z is 2-24; each Y is independently selected from —COCH 2 O— (glycolic ester moiety), —COCH(CH 3 )O— (lactic ester moiety), —COCH 2 OCH 2 CH 2 O— (dioxanone ester moiety), —COCH 2 CH 2 CH 2 CH 2 CH 2 O— (caprolactone ester moiety), —CO(CH 2 ) m O—, where m is 2-4 or 6-24 and —COCH 2 O(CH 2 CH 2 O) n — where n is between 2-24; R′ is hydrogen, benzyl or an alkyl group, the alkyl group being either straight-chained or branched; and p is 1-6. Multi-functional compounds and drug dimers, oligomers and polymers are also disclosed.

  所选化合物包括：DRUG-OH，DRUG-COOH和DRUG-NH2是具有生物活性的化合物；每个X独立选择自—CH2COO—（乙二酸酯基），—CH(CH3)COO—（乳酸酯基），—CH2CH2OCH2COO—（二氧杂环己酮酯基），—CH2CH2CH2CH2CH2COO—（己内酯酯基），—（CH2）yCOO—，其中y为2-4或6-24和—（CH2CH2O）zCH2COO—，其中z为2-24；每个Y独立选择自—COCH2O—（乙二酸酯基），—COCH(CH3)O—（乳酸酯基），—COCH2OCH2CH2O—（二氧杂环己酮酯基），—COCH2CH2CH2CH2CH2O—（己内酯酯基），—CO（CH2）mO—，其中m为2-4或6-24和—COCH2O（CH2CH2O）n—，其中n为2-24；R'为氢，苄基或烷基，所述烷基可以是直链或支链；p为1-6。还公开了多功能化合物和药物二聚体、寡聚体和聚合物。
• Synthesis and Modeling of New Benzofuranone Histone Deacetylase Inhibitors that Stimulate Tumor Suppressor Gene Expression
  作者：Cédric Charrier、Jonathan Clarhaut、Jean-Pierre Gesson、Guillermina Estiu、Olaf Wiest、Joëlle Roche、Philippe Bertrand

  DOI：10.1021/jm9002439

  日期：2009.5.14

  New benzofuranones were synthesized and evaluated toward NCI-H661 non-small cell lung cancer cells. Benzamide derivatives possessed micromolar anti proliferative and histone deacetylase inhibitory activities and modulate histone H4 acetylation. Hydroxamic acids were found to be potent nanomolar anti proliferative agents and HDAC inhibitors. Computational analysis presented a rationale for the activities of the hydroxamate derivatives. Impact of the HDAC inhibition on the expression of E-cadherin and the SEMA3F tumor suppressor genes revealed new promising compounds for lung cancer treatments.
• FUNCTIONALIZED DRUGS AND POLYMERS DERIVED THEREFROM
  申请人：Bezwada Biomedical LLC

  公开号：EP1931334A2

  公开（公告）日：2008-06-18
• FUNCTIONALIZED PHENOLIC COMPOUNDS AND ABSORBABLE THEREFROM
  申请人：Bezwada Biomedical LLC

  公开号：EP1951260A2

  公开（公告）日：2008-08-06