首页> 外国专利> METHOD FOR PREPARING METHYL{4,6-DIAMINO-2-1-(2-FLUOROBENZYL)-1H-PYRAZOLO3,4-BPYRIDINE-3-YLPYRIMIDINE-5-YL}METHYLCARBAMATE AND METHOD FOR PURIFYING THE SAME AS MEDICALLY ACTIVE COMPOUND

METHOD FOR PREPARING METHYL{4,6-DIAMINO-2-1-(2-FLUOROBENZYL)-1H-PYRAZOLO3,4-BPYRIDINE-3-YLPYRIMIDINE-5-YL}METHYLCARBAMATE AND METHOD FOR PURIFYING THE SAME AS MEDICALLY ACTIVE COMPOUND

机译:制备甲基{[4,6-二氨基-2- [1-(2-氟苯甲酸)-1H-吡唑并[3,4-B]吡啶-3-基]嘧啶-5-基}甲基甲酸甲酯的制备方法及纯化方法与医学活性化合物相同

摘要

PROBLEM TO BE SOLVED: To provide a method for preparing methyl{4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]pyrimidine-5-yl}methylcarbamate.;SOLUTION: There is provided a method for synthesizing an aimed methyl carbamate derivative by reacting 2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]-4,5,6-pyrimidine triamine with methyl chloroformate or dimethyl dicarbonate to obtain a pyrimidinyl derivative as an intermediate via a pyridine free reaction pathway and further reacting with methylation agent Me-X.;SELECTED DRAWING: None;COPYRIGHT: (C)2017,JPO&INPIT
机译:解决的问题:提供一种制备甲基{4,6-二氨基-2- [1-(2-氟苄基)-1H-吡唑并[3,4-b]吡啶-3-基]嘧啶-5-的方法基:甲基氨基甲酸酯。;解决方案:提供了一种通过使2- [1-(2-氟苄基)-1H-吡唑并[3,4-b]吡啶-3-基] -4反应合成目标氨基甲酸甲酯的方法。 ,5,6-嘧啶三胺与氯甲酸甲酯或二碳酸二甲酯反应,通过无吡啶反应途径并进一步与甲基化剂Me-X反应,得到嘧啶基衍生物作为中间体。;部分制图:无;版权:(C)2017,日本特许厅

著录项

  • 公开/公告号JP2017081971A

    专利类型

  • 公开/公告日2017-05-18

    原文格式PDF

  • 申请/专利权人 ADVERIO PHARMA GMBH;

    申请/专利号JP20170000073

  • 申请日2017-01-04

  • 分类号C07D471/04;A61K31/506;A61P1/04;A61P7/02;A61P9;A61P9/04;A61P9/06;A61P9/10;A61P9/12;A61P11/06;A61P13/02;A61P13/08;A61P15;A61P15/10;A61P19/10;A61P27/06;

  • 国家 JP

  • 入库时间 2022-08-21 14:01:36

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