Processes for the preparation of 2,3-dihydrothiepine derivatives
    1.
    发明授权
    Processes for the preparation of 2,3-dihydrothiepine derivatives 失效
    2,3-二氢硫嘌呤衍生物的制备方法

    公开(公告)号:US06566535B1

    公开(公告)日:2003-05-20

    申请号:US10019987

    申请日:2001-11-07

    IPC分类号: C07D33712

    CPC分类号: C07D337/08 C07D337/04

    摘要: A process for preparing a compound represented by the following formula: wherein each symbol is as defined below, or a salt thereof, characterized by subjecting a compound represented by the following formula: wherein R1 is an electron-attracting group; R2, R3, R4, R5, R6 and R7 are each a hydrogen atom, a halogen atom, an optionally substituted amino group, an optionally substituted hydroxyl group, an optionally substituted thiol group, an optionally substituted hydrocarbon group, or an optionally substituted heterocyclic group, provided that R6 and R7 may be united to form a ring; and R8 is a hydrogen atom or an optionally substituted hydrocarbon group, or a salt thereof, to a ring-closing reaction.

    摘要翻译: 一种制备由下式表示的化合物的方法:其中每个符号如下所定义,或其盐,其特征在于使下式表示的化合物:其中R1是吸电子基团; R2,R3,R4,R5,R6和R7各自为氢原子,卤素原子,任选取代的氨基,任选取代的羟基,任选取代的硫醇基,任选取代的烃基或任选取代的杂环 组合,条件是R 6和R 7可以结合形成环; 并且R8是氢原子或任选取代的烃基或其盐进行闭环反应。

    Process for producing cyclic compound
    2.
    发明授权
    Process for producing cyclic compound 失效
    环状化合物的制备方法

    公开(公告)号:US07038042B2

    公开(公告)日:2006-05-02

    申请号:US11010215

    申请日:2004-12-10

    IPC分类号: C07D487/00 C07C313/00

    摘要: A process suitable for safely mass-producing, through a short step, cyclic compounds useful in medicines, agricultural chemicals, foods, cosmetics, and chemical products or as intermediates therefor. The process, which is for producing a compound represented by the formula: {wherein Z represents an electron-attracting group; W represents optionally substituted ethylene or optionally substituted vinylene; R3 represents hydrogen or an optionally substituted hydrocarbon group; and X represents a divalent group [provided that when W represents optionally substituted vinylene, then —X—CH2-Z is not —X1—X2—CH2, -Z (wherein X1 represents sulfur or optionally substituted nitrogen and X2 represents optionally substituted ethylene)]} or a salt thereof, is characterized by subjecting a compound represented by the formula (II) or a salt thereof: (wherein the symbols have the same meanings as the above) to a ring closure reaction in a solvent containing a carbonic diester.

    摘要翻译: 一种适用于通过短步安全批量生产用于药物,农药,食品,化妆品和化学产品的环状化合物或其中间体的方法。 该方法用于制备由下式表示的化合物:其中Z表示吸电子基团; W表示任选取代的乙烯或任选取代的亚乙烯基; R 3表示氢或任选取代的烃基; 并且X表示二价基团[条件是当W表示任选取代的亚乙烯基时,则-X-CH 2 -Z不是-X 1 - 2 - -CH 2 - ,其中X 1表示硫或任选取代的氮,X 2表示任选取代的亚乙基)]} 或其盐的特征在于,在含有碳酸二酯的溶剂中使式(II)表示的化合物或其盐(其中符号具有与上述相同的含义)进行闭环反应。

    Process for producing cyclic compound
    4.
    发明申请
    Process for producing cyclic compound 失效
    环状化合物的制备方法

    公开(公告)号:US20050096475A1

    公开(公告)日:2005-05-05

    申请号:US11010215

    申请日:2004-12-10

    摘要: A process suitable for safely mass-producing, through a short step, cyclic compounds useful in medicines, agricultural chemicals, foods, cosmetics, and chemical products or as intermediates therefor. The process, which is for producing a compound represented by the formula: {wherein Z represents an electron-attracting group; W represents optionally substituted ethylene or optionally substituted vinylene; R3 represents hydrogen or an optionally substituted hydrocarbon group; and X represents a divalent group [provided that when W represents optionally substituted vinylene, then —X—CH2-Z is not —X1—X2—CH, -Z (wherein X1 represents sulfur or optionally substituted nitrogen and X2 represents optionally substituted ethylene)]} or a salt thereof, is characterized by subjecting a compound represented by the formula (II) or a salt thereof: (wherein the symbols have the same meanings as the above) to a ring closure reaction in a solvent containing a carbonic diester.

    摘要翻译: 一种适用于通过短步安全批量生产用于药物,农药,食品,化妆品和化学产品的环状化合物或其中间体的方法。 该方法用于制备由下式表示的化合物:其中Z表示吸电子基团; W表示任选取代的乙烯或任选取代的亚乙烯基; R 3表示氢或任选取代的烃基; 并且X表示二价基团[条件是当W表示任选取代的亚乙烯基时,则-X-CH 2 -Z不为-X 1 -X 2 - 其中X 1表示硫或任选取代的氮,X 2表示任选取代的乙烯)]}或其盐,其特征在于: 将含有式(II)的化合物或其盐(其中符号具有与上述相同的含义)与含有碳酸二酯的溶剂进行闭环反应。

    Process for producing cyclic compound
    5.
    发明授权
    Process for producing cyclic compound 失效
    环状化合物的制备方法

    公开(公告)号:US06864367B2

    公开(公告)日:2005-03-08

    申请号:US10204315

    申请日:2001-02-20

    摘要: A process suitable for safely mass-producing, through a short step, cyclic compounds useful in medicines, agricultural chemicals, foods, cosmetics, and chemical products or as intermediates therefor. The process, which is for producing a compound represented by the formula: {wherein Z represents an electron-attracting group; W represents optionally substituted ethylene or optionally substituted vinylene; R3 represents hydrogen or an optionally substituted hydrocarbon group; and X represents a divalent group [provided that when W represents optionally substituted vinylene, then —X—CH2—Z is not —X1—X2—CH2—Z (wherein X1 represents sulfur or optionally substituted nitrogen and X2 represents optionally substituted ethylene)]} or a salt thereof, is characterized by subjecting a compound represented by the formula (II) or a salt thereof: (wherein the symbols have the same meanings as the above) to a ring closure reaction in a solvent containing a carbonic diester.

    摘要翻译: 一种适用于通过短步安全批量生产用于药物,农药,食品,化妆品和化学产品的环状化合物或其中间体的方法。 该方法用于制备由下式表示的化合物:其中Z表示吸电子基团; W表示任选取代的乙烯或任选取代的亚乙烯基; R 3表示氢或任选取代的烃基; 并且X表示二价基团[条件是当W表示任选取代的亚乙烯基时,则-X-CH 2 -Z不是-X 1 -X 2 -CH 2 -Z(其中X 1表示硫或任选取代的 氮和X 2表示任选取代的乙烯)]}或其盐,其特征在于将式(II)表示的化合物或其盐:(其中符号具有与上述相同的含义) 在含有碳酸二酯的溶剂中进行闭环反应。

    Process for preparation of optically active sulfonamides and intermediates for their synthesis
    6.
    发明授权
    Process for preparation of optically active sulfonamides and intermediates for their synthesis 有权
    制备光学活性磺酰胺及其合成中间体的方法

    公开(公告)号:US06982344B2

    公开(公告)日:2006-01-03

    申请号:US10399165

    申请日:2001-10-17

    摘要: A method including resolution of a diastereomeric mixture represented by the formula wherein R1 and R2 are the same or different and each is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group, only one of R1 and R2 contains one asymmetric carbon, and Ra is an optically active and optionally substituted hydrocarbon group or an optically active and optionally substituted heterocyclic group, or a salt thereof, to produce the diastereomer having a steric configuration of the asymmetric carbon for R1 or R2 of an R configuration or an S configuration, or a salt thereof.

    摘要翻译: 一种包括由下式表示的非对映异构体混合物的拆分方法,其中R 1和R 2相同或不同,并且各自为任选取代的烃基或任选取代的杂环 基团中,R 1和R 2中只有一个含有一个不对称碳,R a是光学活性和任选取代的烃基或 光学活性和任选取代的杂环基或其盐,以产生R构型的R 1或R 2的不对称碳的立体构型的非对映异构体或 S构型或其盐。

    Process for producing optically active sulfoxide derivative
    7.
    发明申请
    Process for producing optically active sulfoxide derivative 审中-公开
    光学活性亚砜衍生物的制备方法

    公开(公告)号:US20050107606A1

    公开(公告)日:2005-05-19

    申请号:US10506955

    申请日:2003-03-11

    摘要: A process for preparing an optically active sulfoxide derivative (I) having CCR5 antagonism without causing side reactions such as racemization and Pummerer rearrangement, which comprises reacting a compound (II) with a compound (III) as shown by the following scheme: wherein R1 represents hydrogen, an aliphatic hydrocarbon group or an aromatic group; R2 represents halogeno, alkyl, hydroxyl, amino, an aromatic group, etc.; R3 represents a 5- or 6-membered ring; R4 represents hydrogen, alkyl, alkoxy or halogeno; R5 represents hydrogen, a hydrocarbon group, a heterocyclic group, acyl, etc.; ring A represents an optionally substituted benzene ring; X represents a bond or divalent group comprising a linear part constituted of 1 to 4 atoms; m represents an integer of 1 to 5; n represents an integer of 0 to 3; p represents an integer of 0 to 2; and *1 represents an asymmetric center.

    摘要翻译: 一种制备具有CCR5拮抗作用的光学活性亚砜衍生物(I)的方法,不会引起副反应,例如外消旋化和Pummerer重排,其包括使化合物(II)与化合物(III)反应,如下列方案所示:其中R SUP> 1表示氢,脂族烃基或芳基; R 2表示卤代,烷基,羟基,氨基,芳基等; R 3表示5或6元环; R 4表示氢,烷基,烷氧基或卤代; R 5表示氢,烃基,杂环基,酰基等; 环A表示任选取代的苯环; X表示包含由1至4个原子构成的直链部分的键或二价基团; m表示1〜5的整数, n表示0〜3的整数, p表示0〜2的整数, 和* 1 表示不对称中心。

    Azo Compounds and Process for Production Thereof
    8.
    发明申请
    Azo Compounds and Process for Production Thereof 失效
    偶氮化合物及其制备方法

    公开(公告)号:US20080009539A1

    公开(公告)日:2008-01-10

    申请号:US11661183

    申请日:2005-08-25

    摘要: A process for the production of an aromatic azo compound having a 2,3-dihydrobenzofuran ring bearing a diazo group at the 5-position of the ring by conducting the diazo coupling of a 2,3-dihydrobenzofuran derivative represented by the general formula (II): [wherein R1 and R2 are each independently C1-6 alkyl; R3 is optionally substituted aryl; and R4, R5 and R6 are each independently hydrogen, C1-6 alkyl, halogeno, C1-6 alkoxy, or C1-6 alkylthio] with a benzenediazonium salt having an electron-withdrawing group at the p- and/or o-position in a mixed solvent composed of water and a polar organic solvent.

    摘要翻译: 通过进行由通式(II)表示的2,3-二氢苯并呋喃衍生物的重氮偶联,制备具有环的5-位上具有重氮基的2,3-二氢苯并呋喃环的芳族偶氮化合物的方法 ):[其中R 1和R 2各自独立地为C 1-6烷基; R 3是任选取代的芳基; 和R 4,R 5和R 6各自独立地为氢,C 1-6烷基,卤代, C 1-6烷氧基或C 1-6烷基硫基]与在混合的p-和/或o位上具有吸电子基团的苯二氮鎓盐 溶剂由水和极性有机溶剂组成。

    Method for producing 5'-nucleotide
    9.
    发明授权
    Method for producing 5'-nucleotide 失效
    生产5'-核苷酸的方法

    公开(公告)号:US5623069A

    公开(公告)日:1997-04-22

    申请号:US437984

    申请日:1995-05-10

    CPC分类号: C07H19/04

    摘要: A method of producing 5'-nucleotide, which comprises maintaining a nucleoside suspension in an organic solvent at a temperature not lower than about 20.degree. C., and then subjecting the resultant suspension to a phosphorylatipon of the nucleoside(s).According to the present invention, 5'-nucleotide can be produced from a nucleoside at high purity and high yield in a shortened reaction time, and impurity removal in the nucleotide purification process is easily accomplished.

    摘要翻译: 一种生产5'-核苷酸的方法,其包括在不低于约20℃的温度下将核苷悬浮液保持在有机溶剂中,然后使所得悬浮液经受核苷的磷酸化。 根据本发明,在缩短的反应时间内可以以高纯度和高产率从核苷生产5'-核苷酸,并且容易实现核苷酸纯化过程中的杂质去除。

    Azo compounds and process for production thereof
    10.
    发明授权
    Azo compounds and process for production thereof 失效
    偶氮化合物及其制备方法

    公开(公告)号:US07521545B2

    公开(公告)日:2009-04-21

    申请号:US11661183

    申请日:2005-08-25

    IPC分类号: C07D307/79 C07D405/04

    摘要: A process for the production of an aromatic azo compound having a 2,3-dihydrobenzofuran ring bearing a diazo group at the 5-position of the ring by conducting the diazo coupling of a 2,3-dihydrobenzofuran derivative represented by the general formula (II): [wherein R1 and R2 are each independently C1-6 alkyl; R3 is optionally substituted aryl; and R4, R5 and R6 are each independently hydrogen, C1-6 alkyl, halogeno, C1-6 alkoxy, or C1-6 alkylthio] with a benzenediazonium salt having an electron-withdrawing group at the p- and/or o-position in a mixed solvent composed of water and a polar organic solvent.

    摘要翻译: 通过进行由通式(II)表示的2,3-二氢苯并呋喃衍生物的重氮偶联,制备具有环的5-位上具有重氮基的2,3-二氢苯并呋喃环的芳族偶氮化合物的方法 ):[其中R 1和R 2各自独立地为C 1-6烷基; R3是任选取代的芳基; 和R 4,R 5和R 6各自独立地为氢,C 1-6烷基,卤代,C 1-6烷氧基或C 1-6烷硫基],其中在苯二氮基和/或位置上具有吸电子基团的苯二氮鎓盐 由水和极性有机溶剂组成的混合溶剂。