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(+/-)-3,3,5,5-tetramethyl-2-hydrogeno-2-oxo-[1,4,2]oxazaphosphinane | 945660-98-0

中文名称
——
中文别名
——
英文名称
(+/-)-3,3,5,5-tetramethyl-2-hydrogeno-2-oxo-[1,4,2]oxazaphosphinane
英文别名
2-oxide-3,3,5,5-tetramethyl[1,4,2]oxazaphosphinane;3,3,5,5-Tetramethyl-2-oxido-1,4,2-oxazaphosphinan-2-ium;3,3,5,5-tetramethyl-2-oxido-1,4,2-oxazaphosphinan-2-ium
(+/-)-3,3,5,5-tetramethyl-2-hydrogeno-2-oxo-[1,4,2]oxazaphosphinane化学式
CAS
945660-98-0
化学式
C7H16NO2P
mdl
——
分子量
177.183
InChiKey
FVMUGNZNIFHQHN-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):
    0.1
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    44.3
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    (+/-)-3,3,5,5-tetramethyl-2-hydrogeno-2-oxo-[1,4,2]oxazaphosphinane2-溴氯苯1,1'-双(二苯基膦)二茂铁tris-(dibenzylideneacetone)dipalladium(0)三乙胺 作用下, 以 甲苯 为溶剂, 以144 g的产率得到(±)-2-(2-chlorophenyl)-2-oxo-3,3,5,5-tetramethyl[1,4,2]oxazaphosphinane
    参考文献:
    名称:
    NOVEL PHOSPHINOLACTONE DERIVATIVES AND PHARMACEUTICAL USES THEREOF
    摘要:
    以下式子(I)的化合物:其中:X是O或S;A是芳香(杂)环,由5到10个从碳和氮原子中选择的原子组成,可以是取代基;R′是H或(C1-C6)烷基;R1,R2,R3,R4和R5,相同或不同,由以下组成:H,(C1-C6)烷基和(C6-C10)芳基。该化合物用于治疗神经退行性疾病。
    公开号:
    US20190144476A1
  • 作为产物:
    描述:
    原甲酸三甲酯2,2,4,4-四甲基-1,3-恶唑烷次磷酸 作用下, 以 四氢呋喃甲苯 为溶剂, 反应 18.0h, 以71%的产率得到(+/-)-3,3,5,5-tetramethyl-2-hydrogeno-2-oxo-[1,4,2]oxazaphosphinane
    参考文献:
    名称:
    Phosphinyl analogues of hydroxybupropion: (±)-2-aryl-3,3,5,5-tetramethyl-[1,4,2]-oxazaphosphinanes
    摘要:
    Analogous structures in phosphinate series of hydroxybupropion 2, that is, (+/-)-2-aryl-3,3,5,5-tetramethyl-[1,4,2]-oxazaphosphinanes 8, are prepared according to a two step sequence: addition-cyclization reaction from methyl hypophosphite and oxazolidine 6, followed by a pallado-catalyzed arylation of P-H bond from oxazaphosphinane 7. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2007.05.014
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文献信息

  • Phosphinolactone derivatives and pharmaceutical uses thereof
    申请人:INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)
    公开号:US10947260B2
    公开(公告)日:2021-03-16
    A compound of following formula (I): where: X is O or S; A is an aromatic (hetero)cycle having 5 to 10 atoms selected from among carbon and nitrogen atoms, optionally being substituted; R′ is H or (C1-C6)alkyl group; R1, R2, R3, R4 and R5, the same or different, are selected from the group formed by: H, (C1-C6)alkyl groups and (C6-C10)aryl groups. The compound is for the treatment of neurodegenerative diseases.
    下式(I)的化合物: 其中 X 是 O 或 S; A 是芳香(杂)环,具有 5 至 10 个原子,可从碳原子和氮原子中选择,可选被取代; R′ 是 H 或(C1-C6)烷基; R1、R2、R3、R4 和 R5(相同或不同)选自由以下各项组成的基团:H、(C1-C6)烷基和(C6-C10)芳基。 该化合物用于治疗神经退行性疾病。
  • NOUVEAUX DÉRIVÉS DE PHOSPHINOLACTONES ET LEURS UTILISATIONS PHARMACEUTIQUES
    申请人:Institut National de la Santé et de la Recherche Médicale (INSERM)
    公开号:EP3452489A1
    公开(公告)日:2019-03-13
  • [EN] NOVEL PHOSPHINOLACTONE DERIVATIVES AND PHARMACEUTICAL USES THEREOF<br/>[FR] NOUVEAUX DÉRIVÉS DE PHOSPHINOLACTONES ET LEURS UTILISATIONS PHARMACEUTIQUES
    申请人:INSTITUT NATIONAL DE LA SANTE ET DE LA RECH MEDICALE (INSERM)
    公开号:WO2017191034A1
    公开(公告)日:2017-11-09
    La présente invention concerne un composé de formule (I) suivante : (I), dans laquelle : - X est O ou S; - A est un (hétéro)cycle aromatique comprenant de 5 à 1 0 atomes choisis parmi les atomes de carbone et d'azote, étant éventuellement substitué; - R' est H ou un groupe (C1-C6)alkyle; - R1, R2, R3, R4 et R5, identiques ou différents, sont choisis dans le groupe constitué de : H, des groupes (C1C6)alkyles et des groupes (C6-C10)aryles; pour son utilisation pour le traitement de maladies neurodégénératives.
  • Phosphinyl analogues of hydroxybupropion: (±)-2-aryl-3,3,5,5-tetramethyl-[1,4,2]-oxazaphosphinanes
    作者:Jean-Noël Volle、Nikolay Kaloyanov、Mohamed Chiheb Saada、David Virieux、Jean-Luc Pirat
    DOI:10.1016/j.tetlet.2007.05.014
    日期:2007.7
    Analogous structures in phosphinate series of hydroxybupropion 2, that is, (+/-)-2-aryl-3,3,5,5-tetramethyl-[1,4,2]-oxazaphosphinanes 8, are prepared according to a two step sequence: addition-cyclization reaction from methyl hypophosphite and oxazolidine 6, followed by a pallado-catalyzed arylation of P-H bond from oxazaphosphinane 7. (c) 2007 Elsevier Ltd. All rights reserved.
  • NOVEL PHOSPHINOLACTONE DERIVATIVES AND PHARMACEUTICAL USES THEREOF
    申请人:INSTITUT NATIONAL DE LA SANTE DE LA RECHERCHE MEDICALE (INSERM)
    公开号:US20190144476A1
    公开(公告)日:2019-05-16
    A compound of following formula (I): where: X is O or S; A is an aromatic (hetero)cycle having 5 to 10 atoms selected from among carbon and nitrogen atoms, optionally being substituted; R′ is H or (C 1 -C 6 )alkyl group; R 1 , R 2 , R 3 , R 4 and R 5 , the same or different, are selected from the group formed by: H, (C 1 -C 6 )alkyl groups and (C 6 -C 10 )aryl groups. The compound is for the treatment of neurodegenerative diseases.
    以下式子(I)的化合物:其中:X是O或S;A是芳香(杂)环,由5到10个从碳和氮原子中选择的原子组成,可以是取代基;R′是H或(C1-C6)烷基;R1,R2,R3,R4和R5,相同或不同,由以下组成:H,(C1-C6)烷基和(C6-C10)芳基。该化合物用于治疗神经退行性疾病。
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同类化合物

曲磷胺 曲磷胺 异环磷酰胺杂质F 异环磷酰胺 [(2-羟基-2-氧代-1,4,2-氧氮杂磷杂环己烷-4-基)甲基]膦酸 4-过氧化氢异环磷酰胺 4-氧代异环磷酰胺 4-乙基-7-甲基-7-氮杂-2,6-二氧杂-1-磷杂双环[2.2.2]辛烷1-硫化物 2’-氧代异环磷酰胺 2-[2-氯乙基-[3-(2-氯乙基)-2-氧代-1-氧杂-3-氮杂-2-磷杂环己-2-基]氨基]乙基甲烷磺酸酯 2,3,4,6,7,8-六氢-[1,3,2]氧氮杂膦咛并[2,3-b][1,3,2]氧氮杂膦咛 (2-氯-乙基)-[(R)-3-(2-氯-乙基)-2-氧代-2lambda5-[1,3,2]氧氮杂磷杂环己烷-2-基]-胺 (2R*,4aS*,8aR*)-1-methyl-2-phenyl-1,4,4a,5,6,7,8,8a-octahydro-2H-3,1,2-benzoxazaphosphinine 2-oxide (2S*,4aS*,8aR*)-2-phenyl-1,4,4a,5,6,7,8,8a-octahydro-2H-3,1,2-benzoxazaphosphinine 2-oxide (2R*,4aS*,8aS*)-1-methyl-2-phenyl-1,4,4a,5,6,7,8,8a-octahydro-2H-3,1,2-benzoxazaphosphinine 2-oxide (2S*,4aS*,8aS*)-2-phenyl-1,4,4a,5,6,7,8,8a-octahydro-2H-3,1,2-benzoxazaphosphinine 2-oxide (S,S)-2-oxo-2-propionyl-1,3,2-oxaphosphorinane 2-(Dimethylamino)-3-phenyl-1,3,2-oxazaphosphorinane 2-(1,1,1,3,3,3-Hexafluoroisopropoxy)-3,5,5-trimethyl-1,3,2-oxazaphosphorinane cis-2-(1,1,1,3,3,3-Hexafluoroisopropoxy)-3-methyl-5-tert-butyl-1,3,2-oxazaphosphorinane 2-(1,1,1,3,3,3-Hexafluoroisopropoxy)-3-methyl-1,3,2-oxazaphosphorinane 2-(1,1,1,3,3,3-Hexafluoroisopropoxy)-3-phenyl-1,3,2-oxazaphosphorinane 3,3,5,5-tetramethyl-2-oxido-2-oxo-1,4,2-oxaazaphosphorinane 2-(2-chloroethylamino)-3-(1-methyl-2-chloroethyl)tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxide 4-ethyl-2-hydroxy-2-oxo-tetrahydro-4H-1,4,2-oxazaphosphorine geranyloxyifosfamide 4-methoxy-ifosfamide (2-chloroethyl)-[3-(2-chloroethyl)-2-oxo-4-pentyloxy-2λ5-[1,3,2]oxazaphosphinan-2-yl]amine 3-ethyl-2-hydroxy-2-oxo-1,4,2-oxazaphosphorinane Methyl-[3-(3-methyl-[1,3,2]oxazaphosphinan-2-yloxy)-propyl]-amine 2-Oxo-3-(propan-2-yl)-1,3,2-oxazaphosphinan-2-ium 3-(2-Chloroethyl)-2-(2-chloroethyl)amino-4-hydroxytetrahydro-2H-1,3,2-oxazaphosphorine 3-(2-Chloroethyl)-2-(1-ethyl-2-mesyloxyethylamino)-tetrahydro-2H-1,3,2-oxazaphosphorin-2-oxide 2H-1,3,2-Oxazaphosphorine, 2-fluorotetrahydro-3,5-dimethyl-, 2-oxide 2H-1,3,2-Oxazaphosphorine, 2-fluorotetrahydro-3,4-dimethyl-, 2-oxide (3-Isopropyl-2-oxo-2λ5-[1,3,2]oxazaphosphinan-2-yl)-acetic acid methyl ester cis-2-mesityl-2-oxo-3-phenyl-5-tert-butyl-1,3,2λ5-oxazaphosphorinane trans-2-mesityl-2-oxo-3-phenyl-5-tert-butyl-1,3,2λ5-oxazaphosphorinane (2S,6S)-2-Benzyl-3-(1,1-diethyl-propyl)-6-methyl-[1,3,2]oxazaphosphinane 2-oxide (2R,6S)-2-Benzyl-3-(1,1-diethyl-propyl)-6-methyl-[1,3,2]oxazaphosphinane 2-oxide (2S,6S)-2-((E)-2-Allyloxy-but-2-enyl)-3-tert-butyl-6-methyl-[1,3,2]oxazaphosphinane 2-oxide (2R,6S)-2-((E)-2-Allyloxy-but-2-enyl)-3-tert-butyl-6-methyl-[1,3,2]oxazaphosphinane 2-oxide (S)-(2l,6l)-2-(methoxymethyl)-6-methyl-3-(1-methylethyl)-1,3,2-oxazaphosphorinane 2-sulfide (S)-1-((2S,6S)-3-tert-Butyl-6-methyl-2-oxo-2λ5-[1,3,2]oxazaphosphinan-2-yl)-3-methyl-hex-5-en-2-one 2-methoxy-1,3,2-oxazaphosphinane 3-(2-Chloroethyl-2-<(2-chloroethyl)-(3-mesyloxytrimethylen)-amino>-tetrahydro-2H-1,3,2-oxazaphosphorin-2-oxide 2-chloro-3-[(S)-α-methylbenzyl]tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxide (S)-(2u,6l)-3-(1,1-Diethylpropyl)-6-methyl-2-(2-propenyl)-1,3,2-oxazaphosphorinane 2-oxide 3-(2-chloro-ethyl)-2-(2-hydroxy-ethylamino)-2-oxo-2λ5-[1,3,2]oxazaphosphinan-4-one isopropyl-[3-(3-isopropyl-[1,3,2]oxazaphosphinan-2-yloxy)-propyl]-amine