[2-(4-Nitrophenoxy)-ethoxy]acetic acid methyl ester | 901451-00-1

• 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-Nitrophenoxy)-ethoxy]acetic acid methyl ester
• 英文别名: [2-(4-nitrophenoxy)ethoxy]acetic acid methyl ester；methyl 2-(2-(4-nitrophenoxy)ethoxy)acetate；methyl 2-[2-(4-nitrophenoxy)ethoxy]acetate
• CAS: 901451-00-1
• 化学式: C₁₁H₁₃NO₆
• 分子量: 255.227
• InChiKey: QJMLXJSOGKNWDX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  18
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  90.6
• 氢给体数：
  0
• 氢受体数：
  6

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
  2-(4-硝基苯氧基)乙醇	2-(4-nitrophenoxy)ethanol	16365-27-8	C8H9NO4	183.164
  对硝基苯酚	4-nitro-phenol	100-02-7	C6H5NO3	139.111

• 下游产品

  中文名称	英文名称	CAS号	化学式	分子量
  ——	2-(2-(4-nitrophenoxy)ethoxy)acetic acid	1228792-08-2	C10H11NO6	241.2
  ——	N-methyl-2-(2-(4-nitrophenoxy)ethoxy)ethanamine	1228792-10-6	C11H16N2O4	240.259
  ——	N-methyl-2-(2-(4-nitrophenoxy)ethoxy)acetamide	1228792-09-3	C11H14N2O5	254.243
  ——	[2-(4-Amino-phenoxy)-ethoxy]-acetic Acid Methyl Ester	901451-01-2	C11H15NO4	225.244
  ——	tert-butyl methyl-(2-(2-(4-nitrophenoxy)ethoxy)ethyl)carbamate	1228790-64-4	C16H24N2O6	340.376

反应信息

• 作为反应物：
  描述：

  [2-(4-Nitrophenoxy)-ethoxy]acetic acid methyl ester 在 lithium hydroxide monohydrate 、 盐酸 作用下， 以 乙醇 、 水 为溶剂， 反应 0.5h， 以71%的产率得到2-(2-(4-nitrophenoxy)ethoxy)acetic acid
  参考文献：
  名称：

  [EN] METHODS OF USING SEMI-SYNTHETIC GLYCOPEPTIDES AS ANTIBACTERIAL AGENTS
  [FR] PROCÉDÉS D'UTILISATION DE GLYCOPEPTIDES SEMI-SYNTHÉTIQUES EN TANT QU'AGENTS ANTIBACTÉRIENS

  摘要：

  描述了利用具有抗菌活性的半合成糖肽（化学式I-XIV）的方法。

  公开号：

  WO2011140009A1
• 作为产物：
  描述：

  2-(4-硝基苯氧基)乙醇 、 溴乙酸甲酯 在 sodium hydride 作用下， 以 四氢呋喃 为溶剂， 反应 3.17h， 以68%的产率得到[2-(4-Nitrophenoxy)-ethoxy]acetic acid methyl ester
  参考文献：
  名称：

  [EN] METHODS OF USING SEMI-SYNTHETIC GLYCOPEPTIDES AS ANTIBACTERIAL AGENTS
  [FR] PROCÉDÉS D'UTILISATION DE GLYCOPEPTIDES SEMI-SYNTHÉTIQUES EN TANT QU'AGENTS ANTIBACTÉRIENS

  摘要：

  描述了利用具有抗菌活性的半合成糖肽（化学式I-XIV）的方法。

  公开号：

  WO2011140009A1

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 PHENOLIC COMPOUNDS AND POLYMERS THEREFROM
  申请人：Bezwada Rao S.

  公开号：US20090170927A1

  公开（公告）日：2009-07-02

  The present invention relates to compounds of formula I, which are functionalized phenolic compounds, and polymers formed from the same. Ar—[O—(X) p —R′] q I Polymers formed from the functionalized phenolics are expected to have controllable degradation profiles, enabling them to release an active component over a desired time range. The polymers are also expected to be useful in a variety of medical applications.

  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。
• [EN] NOVEL SEMI-SYNTHETIC GLYCOPEPTIDES AS ANTIBACTERIAL AGENTS<br/>[FR] NOUVEAUX GLYCOPEPTIDES SEMI-SYNTHÉTIQUES COMME AGENTS ANTIBACTÉRIENS
  申请人：LEAD THERAPEUTICS INC

  公开号：WO2010065174A1

  公开（公告）日：2010-06-10

  Semi-synthetic glycopeptides having antibacterial activity are described, in particular, the semi¬ synthetic glycopeptides described herein are made by chemical modification of a glycopeptide (Compound A, Compound B, Compound H or Compound C) or monosaccharide made by hydrolyzing the disaccharide moiety of the amino acid-4 of the parent glycopeptide in acidic medium to give the amino acid-4 monosaccharide; conversion of the monosaccharide to the amino-sugar derivative; acylation of the amino substituent on the amino acid-4 amino-substituted sugar moiety on these scaffolds with certain acyl groups; and conversion of the acid moiety on the macrocyclic ring of these scaffolds to certain substituted amides. Key reaction is the treatment of properly protected intermediate compound with isocyanate. Also provided are methods for the synthesis of the compounds, pharmaceutical compositions containing the compounds, and methods of use of the compounds for the treatment and/or prophylaxis of diseases, especially bacterial infections.

  本文介绍了具有抗菌活性的半合成糖肽，特别是在这里描述的半合成糖肽是通过化学修饰糖肽（化合物A、化合物B、化合物H或化合物C）或通过在酸性介质中水解母体糖肽的氨基酸-4的二糖基团，从而得到氨基酸-4单糖的方法制备的；将单糖转化为氨基糖衍生物；用特定的酰基基团对这些支架上氨基酸-4氨基取代糖基团上的氨基取代基进行酰化；并将这些支架上的大环环上的酸基团转化为某些取代酰胺。关键反应是用异氰酸酯处理适当保护的中间化合物。还提供了合成这些化合物的方法，含有这些化合物的制药组合物以及用于治疗和/或预防疾病，特别是细菌感染的化合物的使用方法。
• Bioabsorbable and biocompatible polyurethanes and polyamides for medical devices
  申请人：S. Bezwada Rao

  公开号：US20060188547A1

  公开（公告）日：2006-08-24

  Absorbable polyurethanes, polyamides and polyester urethanes prepared from at least one compound selected from: or the diamines and diisocyanates thereof, wherein each X represents a member independently selected from —CH 2 COO— (glycolic acid moiety), —CH(CH 3 )COO— (lactic acid moiety), —CH 2 CH 2 OCH 2 COO— (dioxanone), —CH 2 CH 2 CH 2 CH 2 CH 2 COO— (caprolactone moiety), —(CH 2 ) y COO— where y is one of the numbers 2, 3, 4 or 6-24 inclusive, and —(CH 2 CH 2 O) z′ CH 2 COO— where z′ is an integer between 2 and 24, inclusive; each Y represents a member 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), —COCH 2 CH 2 CH 2 CH 2 CH 2 O— (caprolactone ester), —CO(CH 2 ) m O— where m is an integer between 2, 3, 4 or 6-24 inclusive, —COCH 2 O(CH 2 CH 2 O) n — where n is an integer between 2 and 24, inclusive; R′ is hydrogen, benzyl or an alkyl group, the alkyl group being either straight-chained or branched; p is an integer between 1 and 4, inclusive; and Rn represents one or more members selected from H, alkoxy, benzyloxy, aldehyde, halogen, carboxylic acid and —NO 2 , which is attached directly to an aromatic ring or attached through an aliphatic chain. Absorbable polymers prepared from these compounds are useful for drug delivery, tissue engineering, tissue adhesives, adhesion prevention and other implantable medical devices.

  由至少选择自以下化合物制备的可吸收聚氨酯、聚酰胺和聚酯聚氨酯：或其二胺和二异氰酸酯，其中每个X分别代表从—CH2COO—（乙二醇酸基团），—CH（CH3）COO—（乳酸酸基团），—CH2CH2OCH2COO—（二氧环己酮），—CH2CH2CH2CH2CH2COO—（己内酯基团），—（CH2）yCOO—其中y是2、3、4或6-24之间的一个数字，以及—（CH2CH2O）z′CH2COO—其中z′是介于2和24之间的整数；每个Y分别代表从—COCH2O—（乙二醇酸酯基团），—COCH（CH3）O—（乳酸酸酯基团），—COCH2OCH2CH2O—（二氧环己酮酯基团），—COCH2CH2CH2CH2CH2O—（己内酯酯基团），—CO（CH2）mO—其中m是介于2、3、4或6-24之间的整数，—COCH2O（CH2CH2O）n—其中n是介于2和24之间的整数；R′是氢、苄基或烷基，烷基可以是直链或支链；p是介于1和4之间的整数；Rn代表选择自H、烷氧基、苯甲氧基、醛、卤素、羧酸和—NO2的一个或多个成员，它直接附着在芳香环上或通过脂肪链附着。从这些化合物制备的可吸收聚合物对于药物传递、组织工程、组织粘接、粘着预防和其他可植入医疗器械非常有用。
• BIOABSORBABLE AND BIOCOMPATIBLE POLYURETHANES AND POLYAMIDES FOR MEDICAL DEVICES
  申请人：Bezwada Rao S.

  公开号：US20120158127A1

  公开（公告）日：2012-06-21

  Absorbable polyurethanes, polyamides and polyester urethanes prepared from at least one compound selected from: or the corresponding diamines or diisocyanates thereof, wherein each X independently represents —CH 2 COO—, —CH(CH 3 )COO—, —CH 2 CH 2 OCH 2 COO—, —CH 2 CH 2 CH 2 CH 2 CH 2 COO—, —(CH 2 ) y COO— where y is 2 to 4 or 6 to 24, or —(CH 2 CH 2 O) z′ CH 2 COO— where z′ is 2 to 24; each Y represents —COCH 2 O—, —COCH(CH 3 )O—, —COCH 2 OCH 2 CH 2 O—, —COCH 2 CH 2 CH 2 CH 2 CH 2 O—, —CO(CH 2 ) m O— where m is 2 to 4 or 6 to 24, or —COCH 2 O(CH 2 CH 2 O) n — where n is 2 to 24; R′ is hydrogen, benzyl or straight-chained or branched alkyl; p is 1 to 4; and Rn represents one or more members selected from H, alkoxy, benzyloxy, aldehyde, halogen, carboxylic acid and —NO 2 , which is attached directly to an aromatic ring or attached through an aliphatic chain. Absorbable polymers prepared from these compounds are useful for drug delivery, tissue engineering, tissue adhesives, adhesion prevention and other implantable medical devices.

  可吸收的聚氨酯、聚酰胺和聚酯尿素是由至少一种选择自以下化合物或其相应的二胺或二异氰酸酯制备而成：其中每个X独立地表示-CH2COO-、-CH(CH3)COO-、-CH2CH2OCH2COO-、-CH2CH2CH2CH2CH2COO-、-(CH2)yCOO-，其中y为2至4或6至24，或-(CH2CH2O)z'CH2COO-，其中z'为2至24；每个Y表示-COCH2O-、-COCH(CH3)O-、-COCH2OCH2CH2O-、-COCH2CH2CH2CH2CH2O-、-CO(CH2)mO-，其中m为2至4或6至24，或-COCH2O(CH2CH2O)n-，其中n为2至24；R'为氢、苄基或直链或支链烷基；p为1至4；Rn表示选择自H、烷氧基、苄氧基、醛、卤素、羧酸和-NO2的一个或多个成员，它直接附着在芳香环上或通过脂肪链附着。从这些化合物制备的可吸收聚合物可用于药物输送、组织工程、组织粘合剂、粘着预防和其他可植入医疗器械。