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2,4-Dibenzyl-3-oxoglutarsaeuredimethylester | 54813-81-9

中文名称
——
中文别名
——
英文名称
2,4-Dibenzyl-3-oxoglutarsaeuredimethylester
英文别名
Dimethyl-2,4-bis(phenylmethyl)-3-oxoglutarate;dimethyl 2,4-dibenzyl-3-oxopentanedioate
2,4-Dibenzyl-3-oxoglutarsaeuredimethylester化学式
CAS
54813-81-9
化学式
C21H22O5
mdl
——
分子量
354.403
InChiKey
LZXRSFQCNHPGDW-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

物化性质

  • 熔点:
    99-100 °C(Solv: ligroine (8032-32-4))
  • 沸点:
    150 °C(Press: 0.1 Torr)
  • 密度:
    1.168±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    26
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    69.7
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    1,3-丙酮二羧酸二甲酯 以15%的产率得到
    参考文献:
    名称:
    ITO I.; NAGAI S., CHEM. AND PHARM. BULL. , 1974, 22, NO 9, 2131-2135
    摘要:
    DOI:
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文献信息

  • Retroviral protease inhibiting compounds
    申请人:Abbott Laboratories
    公开号:US05142056A1
    公开(公告)日:1992-08-25
    A retroviral protease inhibiting compound of the formula A--X--B or a pharmaceutically acceptable salt, prodrug or ester thereof, wherein X is a linking group; A is (1) substituted amino, (2) substituted carbonyl, (3) functionalized imino, (4) functionalized alkyl, (5) functionalized acyl, (6) functionalized heterocyclic or (7) functionalized (heterocyclic)alkyl; and B is (1) substituted carbonyl independently defined as herein, (2) substituted amino independently defined as herein, (3) functionalized imino independently defined as herein, (4) functionalized alkyl independently defined as herein, (5) functionalized acyl independently defined as herein, (6) functionalized heterocyclic independently defined as herein or (7) functionalized (heterocyclic)alkyl independently defined as herein.
    一种抑制逆转录病毒蛋白酶的化合物,其化学式为A--X--B或其药用盐、前药或酯,其中X为连接基;A为(1)取代基,(2)取代羰基,(3)官能化亚胺基,(4)官能化烷基,(5)官能化酰基,(6)官能化杂环基或(7)官能化(杂环)烷基;B为(1)取代羰基,独立定义如本文所述,(2)取代基,独立定义如本文所述,(3)官能化亚胺基,独立定义如本文所述,(4)官能化烷基,独立定义如本文所述,(5)官能化酰基,独立定义如本文所述,(6)官能化杂环基,独立定义如本文所述或(7)官能化(杂环)烷基,独立定义如本文所述。
  • Intermediates for preparating non-peptide retroviral protease inhibitors
    申请人:ABBOTT LABORATORIES
    公开号:EP0839798A2
    公开(公告)日:1998-05-06
    Intermediates, for preparing non-peptide retroviral protease inhibitors, said intermediates having the formula: or an acid addition salt thereof or an N-protected derivative thereof wherein at each occurrence the N-protecting group is independently selected from the group consisting of formyl, acetyl, pivaloyl, t-butylacetyl, t-butyloxycarbonyl, benzyloxycarbonyl, benzyl and isopropylaminocarbonyl; or said intermediates being selected from: (2S,3R,4S,5S)-2,5-di-(N-(Cbz-valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; (2S,3S,4S,5S)-2,5-di-(N-(Cbz-valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; (2S,3R,4R,5S)-2,5-di-(N-(Cbz-valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; (2S,3S,4S,5S)-2,5-di-(N-(valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; (2S,3R,4S,5S)-2,5-di-(N-(valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; (2S,3R,4R,5S)-2,5-di-(N-(valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; (2S,3S,4R,5S)-2-(N-(t-butyloxy)carbonyl)amino)-5-(N-(Cbz-valinyl)amino)-3,4-dihydroxy-1,6-diphenylhexane; 2-(N-benzyl-N-(benzyloxycarbonyl)amino)-5-(t-butyloxycarbonylamino)-1,6-diphenyl-3-hexene-3,4-oxide; 2-amino-5-(t-butyloxycarbonylamino)-1,6-diphenyl-3-hexene-3,4-oxide; and 2,5-di-(t-butyloxycarbonylamino)-1,6-diphenyl-3-hexene-3,4-oxide; or an acid addition salt thereof.
    用于制备非肽类逆转录病毒蛋白酶抑制剂的中间体,所述中间体具有以下式子: 或其酸加成盐或其 N-保护衍生物,其中每次出现时,N-保护基独立选自甲酰、乙酰、特戊酰、叔丁基乙酰、叔丁氧羰基、苄氧羰基、苄基和异丙基羰基组成的组;或所述中间体选自以下物质 (2S,3R,4S,5S)-2,5-二(N-(Cbz-缬酰)基)-3,4-二羟基-1,6-二苯基己烷; (2S,3S,4S,5S)-2,5-二(N-苄氧羰基缬基)-3,4-二羟基-1,6-二苯基己烷; (2S,3R,4R,5S)-2,5-二(N-苄氧羰基缬基)-3,4-二羟基-1,6-二苯基己烷; (2S,3S,4S,5S)-2,5-二(N-(缬酰)基)-3,4-二羟基-1,6-二苯基己烷; (2S,3R,4S,5S)-2,5-二(N-(缬酰)基)-3,4-二羟基-1,6-二苯基己烷; (2S,3R,4R,5S)-2,5-二(N-(缬酰)基)-3,4-二羟基-1,6-二苯基己烷; (2S,3S,4R,5S)-2-(N-(叔丁氧基)羰基)基)-5-(N-(Cbz-缬酰)基)-3,4-二羟基-1,6-二苯基己烷; 2-(N-苄基-N-(苄氧羰基)基)-5-(叔丁氧羰基基)-1,6-二苯基-3-己烯-3,4-氧化物; 2-基-5-(叔丁氧羰基基)-1,6-二苯基-3-己烯-3,4-氧化物;以及 2,5-二(叔丁氧羰基基)-1,6-二苯基-3-己烯-3,4-氧化物; 或其酸加成盐。
  • US5142056A
    申请人:——
    公开号:US5142056A
    公开(公告)日:1992-08-25
  • US5545750A
    申请人:——
    公开号:US5545750A
    公开(公告)日:1996-08-13
  • US5670675A
    申请人:——
    公开号:US5670675A
    公开(公告)日:1997-09-23
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