摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-(3-methoxypropyl)-4-oxo-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine, 1,1-dioxide | 1206597-14-9

中文名称
——
中文别名
——
英文名称
2-(3-methoxypropyl)-4-oxo-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine, 1,1-dioxide
英文别名
4H-thieno[3,2-e]-1,2-thiazin-4-one, 2,3-dihydro-2-(3-methoxypropyl)-1,1-dioxide;6-chloro 2,3-dihydro-4H-thieno[3,2-e]-1,2-thiazin-4-one-1,1-dioxide;2-(3-methoxypropyl)-1,1-dioxo-3H-thieno[3,2-e]thiazin-4-one
2-(3-methoxypropyl)-4-oxo-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine, 1,1-dioxide化学式
CAS
1206597-14-9
化学式
C10H13NO4S2
mdl
——
分子量
275.35
InChiKey
NTJYCSIIZOCBRX-UHFFFAOYSA-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):
    0.9
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    100
  • 氢给体数:
    0
  • 氢受体数:
    6

文献信息

  • Process for the preparation of (R)-(+)-4-(Ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide.
    申请人:Sathe Dhananjay Govind
    公开号:US20100009977A1
    公开(公告)日:2010-01-14
    Disclosed herein is an improved process for the preparation of (R)-(+)-4-(Ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide (Brinzolamide) and novel intermediates thereof.
    本文披露了一种改进的工艺,用于制备(R)-(+)-4-(乙基基)-3,4-二-2-(3-甲氧基丙基)-2H-噻吩[3,2-e]-1,2-噻嗪-6-磺酰胺-1,1-二化物(布林唑胺)及其新颖的中间体
  • PROCESS FOR THE PREPARATION OF BRINZOLAMIDE
    申请人:Falchi Alessandro
    公开号:US20110118461A1
    公开(公告)日:2011-05-19
    The present invention relates to a process for the preparation of Brinzolamide, or 2H-thieno[3,2-e]-1, 2-thiazin-6-sulfonamide, 4-(ethyl amino)-3, 4-dihydro-2-(3-methoxypropyl)-, 1,1-dioxide,(4R)- via intermediates 2,3-dihydro-4H-thieno[3,2-e]-1, 2-thiazin-4-ones, 1,1-dioxide. Further objects of the present invention are the intermediates mentioned above and other intermediates of the synthesis.
    本发明涉及一种制备布林唑胺或2H-噻吩[3,2-e]-1,2-噻二嗪-6-磺酰胺,4-(乙基基)-3,4-二-2-(3-甲氧基丙基)-1,1-二化物,(4R)的方法,通过中间体2,3-二-4H-噻吩[3,2-e]-1,2-噻二嗪-4-,1,1-二化物。本发明的进一步目的是上述中间体和合成的其他中间体
  • US8344136B2
    申请人:——
    公开号:US8344136B2
    公开(公告)日:2013-01-01
  • [EN] PROCESS FOR THE PREPARATION OF BRINZOLAMIDE<br/>[FR] PROCÉDÉ DE PRÉPARATION DU BRINZOLAMIDE
    申请人:PHF SA
    公开号:WO2010004457A2
    公开(公告)日:2010-01-14
    The present invention relates to a process for the preparation of Brinzolamide, or 2H-thieno [3, 2-e]-1, 2- thiazin-6-sulfonamide, 4-(ethyl amino)-3, 4-dihydro-2-(3- methoxypropyl)-, 1,1-dioxide,(4R)- via intermediates 2, 3-dihydro-4H-thieno [3,2-e]-1, 2-thiazin-4-ones, 1,1- dioxide. Further objects of the present invention are the intermediates mentioned above and other intermediates of the synthesis.
查看更多

同类化合物

布林左胺 布林佐胺盐酸盐 布林佐胺杂质E 布林佐胺杂质C 布林佐胺杂质2 布林佐胺中间体 布林佐胺-d5 布林佐胺 布林佐胺 N-去乙基布林佐胺 6-氯-4-羟基-3,4-二氢-2H-噻吩并[3,2-e][1,2]噻嗪1,1-二氧化物 6-氯-2,3-二氢-4H-噻吩并[3,2-e]-1,2-噻嗪-4-酮1,1-二氧化物 6-乙酰基-1H-噻吩并[2,3-b][1,4]噻嗪-2(3H)-酮 4-羟基-2-甲基-2H-噻吩并[2,3-E]-1,2-噻嗪-3-甲酰胺1,1-二氧化物 3,4-二氢-4-羟基-2H-噻吩并[3,2-e]-1,2-噻嗪-1,1-二氧化物 2-(3-甲氧基丙基)-4-氧代-3,4-二氢-2H-噻吩并[3,2-e][1,2]噻嗪-6-磺酰胺1,1-二氧化物 2,3-二氢-4H-噻吩并[2,3-e][1,2]噻嗪-4-酮1,1-二氧化物 1,5,6-三甲基-1,2,3,4-四氢-2LAMBDA6-噻吩并[2,3-C][1,2]噻嗪-2,2,4-三酮 (S)-6-氯-3,4-二氢-2H-噻吩[3,2-E]-1,2-噻嗪-4-醇 1,1-二氧化氮 (S)-6-氯-2-(3-甲氧基丙基)-3,4-二氢-2H-噻吩并[3,2-e][1,2]噻嗪-4-醇 1,1-二氧化物 (S)-3,4-二氢-4-羟基-2-(3-甲氧丙基)-2H-噻吩并[3,2-E]-1,2-噻嗪-6-磺酰胺 1,1-二氧化物 (4S)-3,4-二氢-2-(3-甲氧基丙基)-2H-噻吩并[3,2-e]-1,2-噻嗪-4-醇 1,1-二氧化物 5,6-Dimethyl-2,3-dihydro-6H-<1,3>thiazin-2-thion (2-Ethyl-1,1-dioxo-1,2-dihydro-1λ6-thieno[3,2-e][1,2]thiazin-3-yl)-methanol 2-Ethyl-3-hydroxymethyl-1,1-dioxo-1,2-dihydro-1λ6-thieno[3,2-e][1,2]thiazine-6-sulfonic acid amide 11-benzylidene-2-methyl-5,5-dioxo-8-phenyl-5,6,7,8-tetrahydro-benzo[2,3]thiepino[4,5-d]thiazolo[3,2-a]pyrimidin-10-one 6-Amidino-2,3-dihydro-1-(2-methylthioethyl)-2-oxothieno[2,3-b][1,4]thiazine hydrochloride 6-Amidino-1-butyl-2,3-dihydro-2-oxo-1H-thieno[2,3-b][1,4]thiazine 4,4-dioxide hydrochloride 2-Morpholino-5-phenyl-thieno<2,3-d><1,3>thiazin-4-on 4-Ethylamino-3,4-dihydro-2-[3-(3-methoxypropylthio)propyl]-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide hydrochloride 3,4-Dihydro-4-[(2-methylpropyl)amino]-2-[(2-methylthio)ethyl]-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 4-Ethylamino-3,4-dihydro-2-[3-(2-methoxyethylthio)propyl]-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 2-(3-methoxypropyl)-4-oxo-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine, 1,1-dioxide 6'-chloro-2',3'-dihydrospiro[1,3-dioxolan-2,4'-thieno[3,2-e][1,2]thiazine], 1',1'-dioxide 3,4-Dihydro-4-propylamino-2-(3-methylthiopropyl)-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 4-Ethylamino-3,4-dihydro-2-(3-ethylthiopropyl)-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 4-Ethylamino-3,4-dihydro-2-[(2-methylthio)ethyl]-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 5-Ethyl-3-dimethylaminomethyl-2H-2,6-methano-3,4,5,6-tetrahydrothieno[3,2-g]-1,2,5-thiadiazocine-8-sulfonamide-1,1-dioxide 4-Ethylamino-3,4-dihydro-2-[3-(3-methoxypropylthio)propyl]-2H-thieno-[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 3-Methylthio-5-methyl-isothiazolo<3',4':2,3>thieno<3,2-d>oxazin-7-on (R)-3,4-dihydro-4-(d5-ethylamino)-2-(3-3d-methoxypropyl)-4H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide 2-(2-Morpholin-4-yl-ethyl)-1,1-dioxo-1,2-dihydro-1λ6-thieno[3,2-e][1,2]thiazine-6-sulfonic acid tert-butylamide 3-hydroxy-2-methyl-4-(2-chlorophenylcarbamoyl)-2H-thieno[3,4-e]-1,2-thiazine 1,1-dioxide [(2R,3R,4R,5S)-2,3,4,5-tetraacetyloxy-6-[[3-[(5R)-3,3-dibutyl-7-(dimethylamino)-1,1-dioxo-4,5-dihydro-2H-1lambda6,4-benzothiazepin-5-yl]phenyl]carbamoylamino]hexyl] acetate N-(1,1-dimethylethyl)-2-[4-(4-morpholinyl)-2-butenyl]-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide 6-ethyl-2-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridin-4-ol 3,4-Dihydro-2-methyl-3-oxo-4-(pyridin-2-yl-carbamoyl)-2H-thieno[2,3-e]1,2-thiazin 1,1-dioxide 3,4-Dihydro-4-hydroxy-N-(1,1-dimethylethyl)-2-[4-(4-morpholinyl)-2-butenyl]-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide