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(S)-N-(2-(4-isopropyl-4,5-dihydrooxazol-2-yl)-6-methoxyphenyl)methanesulfonamide | 546141-34-8

中文名称
——
中文别名
——
英文名称
(S)-N-(2-(4-isopropyl-4,5-dihydrooxazol-2-yl)-6-methoxyphenyl)methanesulfonamide
英文别名
N-[2-[(4S)-4,5-Dihydro-4-(1-methylethyl)-2-oxazolyl]-6-methoxyphenyl]methanesulfonamide;N-[2-methoxy-6-[(4S)-4-propan-2-yl-4,5-dihydro-1,3-oxazol-2-yl]phenyl]methanesulfonamide
(S)-N-(2-(4-isopropyl-4,5-dihydrooxazol-2-yl)-6-methoxyphenyl)methanesulfonamide化学式
CAS
546141-34-8
化学式
C14H20N2O4S
mdl
——
分子量
312.39
InChiKey
YXGJTTRPXOAJEA-LLVKDONJSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    21
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    85.4
  • 氢给体数:
    1
  • 氢受体数:
    6

文献信息

  • INTERMEDIATE FOR PREPARING ERIBULIN MESYLATE AND PROCESS FOR PREPARING THE SAME
    申请人:YONSUNG FINE CHEMICAL CO., LTD.
    公开号:US20200361890A1
    公开(公告)日:2020-11-19
    The present invention relates to a process for preparing a compound of formula (6) which is an intermediate for the preparation of eribulin mesylate with high yields and high purity, and an intermediate therefor.
    本发明涉及一种制备公式(6)化合物的方法,该化合物是制备高产高纯度的依利达唑琼甲磺酸盐的中间体,以及其中间体。
  • [EN] SYNTHETIC PROCESS FOR PREPARATION OF MACROCYCLIC C1-KETO ANALOGS OF HALICHONDRIN B AND INTERMEDIATES USEFUL THEREIN<br/>[FR] PROCÉDÉ DE SYNTHÈSE POUR LA PRÉPARATION D'ANALOGUES C1-CÉTO MACROCYCLIQUES DE L'HALICHONDRINE B ET INTERMÉDIAIRES UTILES DANS CELUI-CI
    申请人:ALPHORA RES INC
    公开号:WO2013142999A1
    公开(公告)日:2013-10-03
    Disclosed is a compound of formula (1), or a pharmaceutically acceptable salt thereof, where R1, R2, R3, R4, R5, R6, R7, R7', R8, R9, R10, R11, R12 and R13 are as disclosed herein. Also, disclosed is a process for the preparation of the compound of formula 1, or a pharmaceutically acceptable salt thereof, and5 intermediates used therein. The compound of formula (1) can be used in the preparation of halichondrin analogs, such as Eribulin; and a process for its preparation from the compound of formula (1) is also disclosed.
    本发明涉及一种式(1)的化合物,或其药学上可接受的盐,其中R1、R2、R3、R4、R5、R6、R7、R7'、R8、R9、R10、R11、R12和R13如本文所述。本发明还涉及一种制备式1化合物或其药学上可接受的盐的工艺及其中间体。式(1)的化合物可用于制备海绵素类似物,例如依利波单;并公开了从式(1)的化合物制备依利波单的工艺。
  • SYNTHETIC PROCESS FOR PREPARATION OF MACROCYCLIC C1-KETO ANALOGS OF HALICHONDRIN B AND INTERMEDIATES USEFUL THEREIN
    申请人:ALPHORA RESEARCH INC.
    公开号:US20150065733A1
    公开(公告)日:2015-03-05
    Disclosed is a compound of formula 1, or a pharmaceutically acceptable salt thereof, where R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 7′ , R 8 , R 9 , R 10 , R 11 , R 12 and R 13 are as disclosed herein. Also, disclosed is a process for the preparation of the compound of formula 1, or a pharmaceutically acceptable salt thereof, and intermediates used therein. The compound of formula 1 can be used in the preparation of halichondrin analogs, such as Eribulin; and a process for its preparation from the compound of formula 1 is also disclosed.
    本文披露了一种公式1的化合物,或其药学上可接受的盐,其中R1、R2、R3、R4、R5、R6、R7、R7'、R8、R9、R10、R11、R12和R13如本文所披露。同时,本文还披露了制备公式1的化合物或其药学上可接受的盐的方法及其中使用的中间体。公式1的化合物可用于制备类海绵毒素类似物,如依杜波林;同时还披露了从公式1的化合物制备依杜波林的方法。
  • SYNTHETIC PROCESS FOR PREPARATION OF MACROCYCLIC C1-KETO ANALOGS OF HALICHONDRIN B AND INTERMEDIATES USEFUL THEREIN INCLUDING INTERMEDIATES CONTAINING -SO2-(P-TOLYL) GROUPS
    申请人:ALPHORA RESEARCH INC.
    公开号:US20160137661A1
    公开(公告)日:2016-05-19
    Disclosed is a compound of formula 1, or a pharmaceutically acceptable salt thereof, where R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 7′ , R 8 , R 9 , R 10 , R 11 , R 12 and R 13 are as disclosed herein. Also, disclosed is a process for the preparation of the compound of formula 1, or a pharmaceutically acceptable salt thereof, and intermediates used therein. The compound of formula 1 can be used in the preparation of halichondrin analogs, such as Eribulin; and a process for its preparation from the compound of formula 1 is also disclosed.
    本文公开了式子1的化合物或其药学上可接受的盐,其中R1、R2、R3、R4、R5、R6、R7、R7'、R8、R9、R10、R11、R12和R13如本文所述。本文还公开了制备式子1的化合物或其药学上可接受的盐的方法以及其中使用的中间体。式子1的化合物可用于制备半乳霉素类似物,例如依利妥珠单抗;并且还公开了从式子1的化合物制备依利妥珠单抗的方法。
  • INTERMEDIATE FOR PREPARING ERIBULIN MESYLATE AND METHOD FOR PREPARING SAME
    申请人:Yonsung Fine Chemical Co., Ltd.
    公开号:EP3712141A1
    公开(公告)日:2020-09-23
    The present invention relates to a process for preparing a compound of formula (6) which is an intermediate for the preparation of eribulin mesylate with high yields and high purity, and an intermediate therefor.
    本发明涉及一种制备式(6)化合物的工艺及其中间体,该式(6)化合物是制备甲磺酸埃里布林的高产率和高纯度中间体。
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