benzyl 5-(4-methyl-piperazin-1-ylmethyl)-1,3-dihydro-isoindole-2-carboxylate | 1019890-05-1

• 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: benzyl 5-(4-methyl-piperazin-1-ylmethyl)-1,3-dihydro-isoindole-2-carboxylate
• 英文别名: 5-(4-Methyl-piperazin-1-ylmethyl)-1,3-dihydro-isoindole-2-carboxylic acid benzyl ester；benzyl 5-[(4-methylpiperazin-1-yl)methyl]-1,3-dihydroisoindole-2-carboxylate
• CAS: 1019890-05-1
• 化学式: C₂₂H₂₇N₃O₂
• 分子量: 365.475
• InChiKey: NXWBAUDMOGSZNF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  27
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  36
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  benzyl 5-(4-methyl-piperazin-1-ylmethyl)-1,3-dihydro-isoindole-2-carboxylate 在 palladium 10% on activated carbon 氢气 作用下， 以 甲醇 为溶剂， 反应 2.5h， 生成 2,3-二氢-5-[(4-甲基-1-哌嗪基)甲基]-1H-异吲哚
  参考文献：
  名称：

  WO2008/44029

  摘要：

  公开号：
• 作为产物：
  描述：

  5-(4-methyl-piperazin-1-ylmethyl)-1,3-dihydro-isoindole-2-carboxylic acid benzyl ester dihydrochloride 在 potassium carbonate 作用下， 以 水 、 乙酸乙酯 为溶剂， 生成 benzyl 5-(4-methyl-piperazin-1-ylmethyl)-1,3-dihydro-isoindole-2-carboxylate
  参考文献：
  名称：

  WO2008/44029

  摘要：

  公开号：

文献信息

• [EN] PHARMACEUTICAL COMPOUNDS<br/>[FR] COMPOSÉS PHARMACEUTIQUES
  申请人：ASTEX THERAPEUTICS LTD

  公开号：WO2009125230A1

  公开（公告）日：2009-10-15

  The invention provides a compound of the formula (1 ): or a salt, solvate, N-oxide or tautomer thereof; wherein either R1 is R1a and R2 is R2a; or R1 is R1b and R2 is R2b; provided that in each case at least one of R1 and R2 is other than hydrogen; R1a and R2a are the same or different and each is selected from hydrogen, C1-4 alkyl, C2-4 alkenyl and C2-4 alkynyl wherein the C1-4 alkyl is optionally substituted by C1-2 alkoxy; R1b and R2b are the same or different and are selected from hydrogen, C(O)NR4R5, C(O)R6 and C(O)OR6 where R6 is C1-4 alkyl, R4 and R5 are both C1-4 alkyl, or NR4R5 forms a 4 to 7 membered saturated heterocyclic ring optionally containing a second heteroatom ring member selected from O, N or S and oxidised forms of N and S, the heterocyclic ring being optionally substituted by one or two C1-4 alkyl groups and/or one or two oxo groups; and R3 is a group (D): wherein the asterisk denotes the point of attachment to the isoindoline ring; but excluding acetic acid 5-acetoxy-4-isopropyl-2-[5-(4-methyl-piperazin-1 -ylmethyl)-1,3- dihydro-isoindole-2-carbonyl]-phenyl ester.

  该发明提供了一个化合物，其化学式为（1）：或其盐、溶剂合物、N-氧化物或互变异构体；其中R1是R1a且R2是R2a；或R1是R1b且R2是R2b；但在每种情况下，R1和R2中至少有一个不是氢；R1a和R2a相同或不同，每个都选自氢、C1-4烷基、C2-4烯基和C2-4炔基，其中C1-4烷基可选择地被C1-2烷氧基取代；R1b和R2b相同或不同，选自氢、C（O）NR4R5、C（O）R6和C（O）OR6，其中R6是C1-4烷基，R4和R5都是C1-4烷基，或NR4R5形成一个含有第二杂原子环成员O、N或S和氮和硫的氧化形式的4到7成员饱和杂环，该杂环可选择地被一个或两个C1-4烷基基团和/或一个或两个氧基团取代；R3是一个基团（D）：其中星号表示与异吲哚啉环的连接点；但不包括乙酸5-乙氧基-4-异丙基-2-[5-(4-甲基哌嗪-1-基甲基)-1,3-二氢-异吲哚-2-羰基]-苯基酯。
• PHARMACEUTICAL COMPOUNDS
  申请人：Congreve Miles Stuart

  公开号：US20100152184A1

  公开（公告）日：2010-06-17

  The invention provides a compound for use in medicine, the compound being a compound of the formula (VI 0 ) or a salt, solvate, tautomer or N-oxide thereof: wherein the bicyclic group: is selected from the structures C1, C5 and C6: wherein n is 0, 1, 2 or 3; R 1 is hydrogen, hydroxy, or O—R z ; R 2a is hydroxy, methoxy or O—R z ; provided that at least one of R 1 and R 2a is O—R z ; R z is L p -R p1 ; SO 3 H; a glucuronide residue; a mono-, di- or tripeptide residue; or L p is a bond, C═O, (C═O)O, (C═O)NR p1 or S(O) x NR p1 ; x is 1 or 2; R p1 is hydrogen or a an optionally substituted C 1-25 hydrocarbyl group containing 0, 1 or 2 carbocyclic rings and 0, 1, 2, 3, 4, 5 or 6 carbon-carbon multiple bonds, provided that R p1 is not hydrogen when L p is a bond, C═O or (C═O)O; and provided also that O—R z does not contain an O—O moiety; and excluding compounds wherein R 1 is hydroxy and R 2a is methoxy; R p2 and R p3 are the same or different and each is a group R p1 ; and R 3 , R 4a , R 8 and R 10 are defined in the claims. The compounds of formula (VI 0 ) are pro-drugs of parent compounds wherein R 1 and/or R 2a are hydroxy, wherein the parent compounds have Hsp90 inhibiting activity.

  本发明提供了一种用于药物中的化合物，该化合物是式(VI0)的化合物或其盐、溶剂化物、互变异构体或N-氧化物：其中双环基团：选自结构C1、C5和C6：其中n为0、1、2或3；R1为氢、羟基或O—Rz；R2a为羟基、甲氧基或O—Rz；条件是R1和R2a中至少一个是O—Rz；Rz为Lp-Rp1；SO3H；一个葡萄糖苷酸残基；一个单、二或三肽残基；或Lp为键、C═O、(C═O)O、(C═O)NRp1或S(O)xNRp1；x为1或2；Rp1为氢或一个可选地取代的含0、1或2个碳环和0、1、2、3、4、5或6个碳-碳多重键的C1-25烃基团，条件是当Lp为键、C═O或(C═O)O时，Rp1不是氢；并且还条件是O—Rz不包含O—O部分；并排除R1为羟基且R2a为甲氧基的化合物；Rp2和Rp3相同或不同，且各自为Rp1基团；R3、R4a、R8和R10如权利要求中定义。式(VI0)的化合物是其中R1和/或R2a为羟基的母化合物的前药，其中母化合物具有Hsp90抑制活性。
• HYDROBENZAMIDE DERIVATIVES AS INHIBITORS OF HSP90
  申请人：Frederickson Martyn

  公开号：US20110046155A1

  公开（公告）日：2011-02-24

  The invention provides an acid addition salt of a compound of the formula (1) Also provided by the invention are processes for preparing the compound of formula (1) and alkyl analogues thereof, novel intermediates for use in the process and methods for preparing the intermediates. The invention also provides new medical uses of compounds of the formula (1) and its ethyl analogue.

  该发明提供了化合物（1）的酸加成盐。该发明还提供了制备化合物（1）及其烷基类似物的方法，用于该过程的新型中间体以及制备中间体的方法。该发明还提供了化合物（1）及其乙基类似物的新医药用途。
• PHARMACEUTICAL COMBINATIONS
  申请人：Gallagher Neil James

  公开号：US20100092474A1

  公开（公告）日：2010-04-15

  The invention provides combinations comprising (or consisting essentially of) one or more ancillary compound(s) and a compound of the formula (I): or salts, tautomers, solvates and N-oxides thereof; wherein R 1 is hydroxy or hydrogen; R 2 is hydroxy; methoxy or hydrogen; provided that at least one of R 1 and R 2 is hydroxy; R 3 is selected from hydrogen; halogen; cyano; optionally substituted C 1-5 hydrocarbyl and optionally substituted C 1-5 hydrocarbyloxy; R 4 is selected from hydrogen; a group —(O) n —R 7 where n is 0 or 1 and R 7 is an optionally substituted acyclic C 1-5 hydrocarbyl group or a monocyclic carbocyclic or heterocyclic group having 3 to 7 ring members; halogen; cyano; hydroxy; amino; and optionally substituted mono- or di-C 1-5 hydrocarbyl-amino; or R 3 and R 4 together form a monocyclic carbocyclic or heterocyclic ring of 5 to 7 ring members; and NR 5 R 6 forms an optionally substituted bicyclic heterocyclic group having 8 to 12 ring members of which up to 5 ring members are heteroatoms selected from oxygen, nitrogen and sulphur. The combinations have activity as Hsp90 inhibitors.

  本发明提供的组合物包括（或者基本上由）一种或多种辅助化合物和一个式（I）的化合物组成，或其盐，互变异构体，溶剂化物和N-氧化物；其中R1是羟基或氢原子；R2是羟基，甲氧基或氢原子；至少R1和R2中的一个是羟基；R3选自氢原子，卤素，氰基，可选取代的C1-5烃基和可选取代的C1-5烃氧基；R4选自氢原子，一个—（O）n—R7基团，其中n为0或1，R7是一个可选取代的无环C1-5烃基基团或一个具有3至7个环成员的单环碳环或杂环基团；卤素，氰基，羟基，氨基和可选取代的单一或二元C1-5烃基氨基；或者R3和R4共同形成一个有5至7个环成员的单环碳环或杂环；并且NR5R6形成一个有8至12个环成员的可选取代的双环杂环基团，其中最多有5个环成员是从氧，氮和硫中选取的杂原子。这些组合物具有作为Hsp90抑制剂的活性。
• Pharmaceutical combinations
  申请人：Astex Therapeutics Limited

  公开号：US08277807B2

  公开（公告）日：2012-10-02

  The invention provides combinations comprising (or consisting essentially of) one or more ancillary compound(s) and a compound of the formula (I): or salts, tautomers, solvates and N-oxides thereof; wherein R1 is hydroxy or hydrogen; R2 is hydroxy; methoxy or hydrogen; provided that at least one of R1 and R2 is hydroxy; R3 is selected from hydrogen; halogen; cyano; optionally substituted C1-5 hydrocarbyl and optionally substituted C1-5 hydrocarbyloxy; R4 is selected from hydrogen; a group —(O)n—R7 where n is 0 or 1 and R7 is an optionally substituted acyclic C1-5 hydrocarbyl group or a monocyclic carbocyclic or heterocyclic group having 3 to 7 ring members; halogen; cyano; hydroxy; amino; and optionally substituted mono- or di-C1-5 hydrocarbyl-amino; or R3 and R4 together form a monocyclic carbocyclic or heterocyclic ring of 5 to 7 ring members; and NR5R6 forms an optionally substituted bicyclic heterocyclic group having 8 to 12 ring members of which up to 5 ring members are heteroatoms selected from oxygen, nitrogen and sulphur. The combinations have activity as Hsp90 inhibitors.

  本发明提供了组合物，包括(或基本上由)一个或多个辅助化合物和式(I)的化合物组成：或其盐、互变异构体、溶剂化物和N-氧化物；其中R1是羟基或氢；R2是羟基、甲氧基或氢；但至少其中之一为羟基；R3选择自氢、卤素、氰基、可选取代的C1-5烃基和可选取代的C1-5烃氧基；R4选择自氢、—(O)n—R7基团，其中n为0或1，R7是可选取代的无环C1-5烃基团或具有3至7个环成员的单环碳环或杂环基团；卤素、氰基、羟基、氨基和可选取代的单或双C1-5烃基氨基；或R3和R4共同形成5至7个环成员的单环碳环或杂环环；NR5R6形成8至12个环成员的可选取代的双环杂环基团，其中最多5个环成员为氧、氮和硫的杂原子。这些组合物具有作为Hsp90抑制剂的活性。