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17-<(E)-isocyano(tosyl)methylene>-3-methoxyandrosta-3,5-diene | 93206-67-8

中文名称
——
中文别名
——
英文名称
17-<(E)-isocyano(tosyl)methylene>-3-methoxyandrosta-3,5-diene
英文别名
(E)-17-(isocyanotosylmethylene)-3-methoxyandrosta-3,5-diene;17-[(E)-isocyano(tosyl)methylene]-3-methoxyandrosta-3,5-diene;(8R,9S,10R,13S,14S,17E)-17-[isocyano-(4-methylphenyl)sulfonylmethylidene]-3-methoxy-10,13-dimethyl-1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthrene
17-<(E)-isocyano(tosyl)methylene>-3-methoxyandrosta-3,5-diene化学式
CAS
93206-67-8
化学式
C29H35NO3S
mdl
——
分子量
477.668
InChiKey
JHLSFNSIQCXBTN-OGGPIXAQSA-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):
    6.1
  • 重原子数:
    34
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    56.1
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis of 17-(2-Methoxy-3-oxazolin-4-yl)-, 17-(3-Oxazolin-4-yl)-, and 17-(2-Oxazolin-4-ylidene) Substituted Steroids and Their Use as Precursors of Corticosteroids
    摘要:
    17-(Isocyanotosylmethylene)steroids 4 are useful intermediates in the conversion of 17-oxosteroids into 17-(hydroxyacetyl)steroids. The 21-CH2OH group is effectively introduced by a base-mediated reaction of compounds 4 with formaldehyde and MeOH to give 17-(2-methoxy-3-oxazolin-4-yl) derivatives 12, which by acid hydrolysis give 17-(hydroxyacetyl)steroids 10 and 16 in high yields. Partial hydrolysis of the same oxazoline derivatives 12 provides the 17-(hydroxyacetyl) cortico side chain of 13 equipped with a formyl-protected hydroxy group. 3-Oxazolinyl and 2-oxazolinylidene steroid derivatives 19, 20, and 21, without a 2-methoxy substituent, are discussed as alternatives of 12.
    DOI:
    10.1021/jo00098a024
  • 作为产物:
    参考文献:
    名称:
    Leusen, Daan van; Leusen, Albert M. van, Recueil des Travaux Chimiques des Pays-Bas, 1991, vol. 110, # 10, p. 393 - 401
    摘要:
    DOI:
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文献信息

  • Synthesis of 20-oxo steroids
    作者:Daan van Leusen、Erik van Echten、Albert M. van Leusen
    DOI:10.1002/recl.19921111102
    日期:——
    The synthesis is described of a series of eighteen 16-dehydro-20-isocyano-20-sulfonylpregnanes (5 and 8–14) by C-20 alkylation of 17-[isocyano(sulfonyl)methylene]androstanes 1–3. The geminal isocyano and sulfonyl groups at C-20 (compounds 5, 8–14) are removed by acid hydrolysis to provide a new entry into 20-oxo steroids (6, 15–19). The C-20 alkylation also includes halomethylation and alkoxymethylation
    通过17- [异基(磺酰基)亚甲基] Androstanes 1-3的C-20烷基化反应,描述了18个16-脱氢-20-异基20-磺酰基孕烯的合成(5和8-14)。通过酸解将C-20上的双异氰酸酯基和磺酰基基团(化合物5、8–14)除去,以提供新的进入20-氧代类固醇的能力(6、15–19)。C-20烷基化还包括卤甲基化和烷氧基甲基化,以分别形成21-卤-和21-烷氧基-16-脱氢-20-氧杂戊烷。作为酸解的一种有吸引力的替代方法,首先用Pb(OAc)4氧化异解成异氰酸酯基之前(双异氰酸酯基和磺酰基基团)解成相同的20-氧代甾族化合物 后一种转化是在室温下在非酸性条件下在氧化铝在二氯甲烷中的浆液中进行的。
  • New process for the preparation of 20-keto-delta-16-steroids and new intermediate compounds formed in this process
    申请人:GIST-BROCADES N.V.
    公开号:EP0123735A1
    公开(公告)日:1984-11-07
    The invention relates to a new process for the introduction into steroids of a 17-side chains containing a 20-keto group under the simultaneously formation of an unsaturated bond between C,6 and C17 by reaction of 17-(isocyano- sulfonylmethylene)-steroids with an alkylating agent to 20-isocyano-20-sulfonyl-delta16-steroids, followed by hydrolysis of these latter compounds to 20-keto-delta16-steroids. The invention also relates to the intermediate compounds which are formed in this process, i.e. 20-isocyano-20-sulfonyl-delta16-steroids and to the ultimately formed 20- keto-delta16-steroids, as far as these latter compounds are new.
    本发明涉及一种在C,6和C17之间同时形成不饱和键的情况下,将含有20-酮基的17-侧链引入类固醇的新工艺,其方法是将17-(异基-磺酰亚甲基)类固醇与烷化剂反应生成20-异基-20-磺酰亚甲基-δ16-类固醇,然后将这些化合物解生成20-酮酰亚甲基-δ16-类固醇。本发明还涉及在此过程中形成的中间化合物,即 20-异基-20-磺酰基-δ16-类固醇和最终形成的 20-酮基-δ16-类固醇,只要后一种化合物是新的。
  • New process for the preparation of 21-hydroxy-20-keto-delta 16-steroids and new intermediate compounds formed in this process
    申请人:GIST-BROCADES N.V.
    公开号:EP0123736A1
    公开(公告)日:1984-11-07
    The invention relates to a new process for the preparation of 21-hydroxy-20-keto-steroids from 17-isocyano-sulfonylmethylene-steroids whereby simultaneously an unsaturated bond is introduced between C16 and C17. Furthermore, the invention relates to new intermediate compounds formed in this process and their preparation.
    本发明涉及一种从 17-异基磺酰亚甲基类固醇制备 21-羟基-20-酮类固醇的新工艺,在该工艺中,同时在 C16 和 C17 之间引入不饱和键。此外,本发明还涉及在该工艺中形成的新中间化合物及其制备方法。
  • A novel method to build acetyl and hydroxyacetyl side-chains in 17-oxosteroids
    作者:Daan van Leusen、Albert M. van Leusen
    DOI:10.1016/s0040-4039(01)81236-3
    日期:1984.1
  • Van Leusen; Van Leusen, Synthesis, 1991, # 7, p. 531 - 532
    作者:Van Leusen、Van Leusen
    DOI:——
    日期:——
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同类化合物

(5β)-17,20:20,21-双[亚甲基双(氧基)]孕烷-3-酮 (5α)-2′H-雄甾-2-烯并[3,2-c]吡唑-17-酮 (3β,20S)-4,4,20-三甲基-21-[[[三(异丙基)甲硅烷基]氧基]-孕烷-5-烯-3-醇-d6 (25S)-δ7-大发酸 (20R)-孕烯-4-烯-3,17,20-三醇 (11β,17β)-11-[4-({5-[(4,4,5,5,5-五氟戊基)磺酰基]戊基}氧基)苯基]雌二醇-1,3,5(10)-三烯-3,17-二醇 齐墩果酸衍生物1 黄麻属甙 黄芪皂苷III 黄芪皂苷 II 黄芪甲苷 IV 黄芪甲苷 黄肉楠碱 黄果茄甾醇 黄杨醇碱E 黄姜A 黄夹苷B 黄夹苷 黄夹次甙乙 黄夹次甙乙 黄夹次甙丙 黄体酮环20-(乙烯缩醛) 黄体酮杂质EPL 黄体酮杂质1 黄体酮杂质 黄体酮杂质 黄体酮EP杂质M 黄体酮EP杂质G(RRT≈2.53) 黄体酮EP杂质F 黄体酮6-半琥珀酸酯 黄体酮 17alpha-氢过氧化物 黄体酮 11-半琥珀酸酯 黄体酮 麦角甾醇葡萄糖苷 麦角甾醇氢琥珀酸盐 麦角甾烷-6-酮,2,3-环氧-22,23-二羟基-,(2b,3b,5a,22R,23R,24S)-(9CI) 麦角甾烷-3,6,8,15,16-五唑,28-[[2-O-(2,4-二-O-甲基-b-D-吡喃木糖基)-a-L-呋喃阿拉伯糖基]氧代]-,(3b,5a,6a,15b,16b,24x)-(9CI) 麦角甾烷-26-酸,5,6:24,25-二环氧-14,17,22-三羟基-1-羰基-,d-内酯,(5b,6b,14b,17a,22R,24S,25S)-(9CI) 麦角甾-8-烯-3-醇 麦角甾-8,24(28)-二烯-26-酸,7-羟基-4-甲基-3,11-二羰基-,(4a,5a,7b,25S)- 麦角甾-7,22-二烯-3-酮 麦角甾-7,22-二烯-17-醇-3-酮 麦角甾-5,24-二烯-26-酸,3-(b-D-吡喃葡萄糖氧基)-1,22,27-三羟基-,d-内酯,(1a,3b,22R)- 麦角甾-5,22,25-三烯-3-醇 麦角甾-4,6,8(14),22-四烯-3-酮 麦角甾-1,4-二烯-3-酮,7,24-二(乙酰氧基)-17,22-环氧-16,25-二羟基-,(7a,16b,22R)-(9CI) 麦角固醇 麦冬皂苷D 麦冬皂苷D 麦冬皂苷 B