tert-butyl N-[(1R,3S,4S,5S,6S)-4,5-dihydroxy-7-oxabicyclo[4.1.0]heptan-3-yl]carbamate | 205499-13-4

• 分子结构分类: 有机化合物 - 有机杂环化合物
• 英文名称: tert-butyl N-[(1R,3S,4S,5S,6S)-4,5-dihydroxy-7-oxabicyclo[4.1.0]heptan-3-yl]carbamate
• CAS: 205499-13-4
• 化学式: C₁₁H₁₉NO₅
• 分子量: 245.276
• InChiKey: NZTHJLUHDBSSDF-QKAWAISNSA-N

物化性质

• 沸点：
  411.341±45.00 °C(Press: 760.00 Torr)(predicted)
• 密度：
  1.300±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  -0.4
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  91.3
• 氢给体数：
  3
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  tert-butyl N-[(1R,3S,4S,5S,6S)-4,5-dihydroxy-7-oxabicyclo[4.1.0]heptan-3-yl]carbamate 在 吡啶 、 4-二甲氨基吡啶 、 正丁基锂 、 双氧水 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 为溶剂， 反应 33.75h， 生成 [(1R,4S,5S,6R)-5,6-diacetyloxy-4-[(2-methylpropan-2-yl)oxycarbonylamino]cyclohex-2-en-1-yl] acetate
  参考文献：
  名称：

  Synthesis of Conduramines from N-tert-Butoxycarbonylpyrrole

  摘要：

  Two related synthetic strategies were devised to convert the Diels-Alder adduct 3c of Boc-pyrrole and p-toluenesulfonylacetylene into various racemic and optically pure conduramines. One process consists of the regio-and stereoselective hydroxylation of 3c to the tri-and dihydroxylated azabicyclo[2.2.1]heptane derivatives 10b (Scheme 2) and the exo-endo mixture 13-14 (Scheme 3). Anionic fragmentation of 10b (methylmagnesium bromide) and of the 13-14 sulfone mixture (lithium bis(trimethylsilyl)amide) generated the corresponding tri-and dihydroxylated aminocyclohexenes 17 and 16 (Scheme 3). Compound 17 is an aminocyclitol with a stereochemistry and partial aminotriol sequence identical to that found in neoinosamine. Compound 16 served as a source of the protected and fi ee aminodiols 35b, and 35a (Scheme 6), which were stereospecifically epoxidized to 36 (Scheme 6) and 40 (Scheme 7). Phenylselenide cleavage of these epoxides provided 37 (Scheme 6) and 41a (Scheme 7), which after selenoxide cycloelimination and protecting group manipulation were converted into (+/-)-conduramine C-l (39a, Scheme 6) and the previously unreported, all-cis-conduramine D-l (43a, Scheme 7). In a second process, anionic fragmentaion of the bicyclic system is effected prior to introduction of the hydroxyl groups, as exemplified by the high-yielding conversion of the exo-endo mixture of azabicycloheptenes 11 and 12 into the aminocyclohexadiene 15 (Scheme 3). Osmate catalyzed cis-dihydroxylation of the derived bis-Boc derivative 20 (Scheme 4) Zed stereospecifically to the alpha-cis-diol 21 which was transformed into (+/-)-conduramine A-1 (27a) and its tetraacetyl derivative 27b via the epoxy compound 24. On the other hand, peracid oxidation of the diene 15 gave the beta-epoxide 28 (Scheme 5) which was cleaved to the trans-diol 29 with aqueous sulfuric acid. This diol was converted into (+/-)-conduramine F-1(34a) and its tetraacetyl derivative (34b) by a reaction sequence similar to that used for the other conduramine syntheses. Fractional crystallization of the diastereomeric mixture of Michael adducts obtained from (+/-)-3c and (-)methyl lactate gave (-)-44a and (-)-45a both in greater than or equal to 47% yield (Scheme 8). Both the carboxylic acid (+)-44b and the primary alcohol (+)-46 derived from (-)-44a were converted into (-)-3c with excess methylmagnesium bromide (ca. 40% overall yield). In the same way (-)-45a was transformed into optically pure (+)-3c. (-)-3c and (+)-3c were then converted into (-)-conduramine C-l [(-)-39a] and (+)-conduramine D-l [(+)-43a] by procedures identical to those used for the racemic compounds.

  DOI：

  10.1021/jo971907r
• 作为产物：
  描述：

  [(1S,5R,6S)-5,6-Dihydroxy-3-(toluene-4-sulfonyl)-cyclohex-3-enyl]-carbamic acid tert-butyl ester 在 disodium hydrogenphosphate 、 sodium amalgam 、 碳酸氢钠 、 间氯过氧苯甲酸 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 为溶剂， 反应 17.0h， 生成 tert-butyl N-[(1R,3S,4S,5S,6S)-4,5-dihydroxy-7-oxabicyclo[4.1.0]heptan-3-yl]carbamate
  参考文献：
  名称：

  Synthesis of Conduramines from N-tert-Butoxycarbonylpyrrole

  摘要：

  Two related synthetic strategies were devised to convert the Diels-Alder adduct 3c of Boc-pyrrole and p-toluenesulfonylacetylene into various racemic and optically pure conduramines. One process consists of the regio-and stereoselective hydroxylation of 3c to the tri-and dihydroxylated azabicyclo[2.2.1]heptane derivatives 10b (Scheme 2) and the exo-endo mixture 13-14 (Scheme 3). Anionic fragmentation of 10b (methylmagnesium bromide) and of the 13-14 sulfone mixture (lithium bis(trimethylsilyl)amide) generated the corresponding tri-and dihydroxylated aminocyclohexenes 17 and 16 (Scheme 3). Compound 17 is an aminocyclitol with a stereochemistry and partial aminotriol sequence identical to that found in neoinosamine. Compound 16 served as a source of the protected and fi ee aminodiols 35b, and 35a (Scheme 6), which were stereospecifically epoxidized to 36 (Scheme 6) and 40 (Scheme 7). Phenylselenide cleavage of these epoxides provided 37 (Scheme 6) and 41a (Scheme 7), which after selenoxide cycloelimination and protecting group manipulation were converted into (+/-)-conduramine C-l (39a, Scheme 6) and the previously unreported, all-cis-conduramine D-l (43a, Scheme 7). In a second process, anionic fragmentaion of the bicyclic system is effected prior to introduction of the hydroxyl groups, as exemplified by the high-yielding conversion of the exo-endo mixture of azabicycloheptenes 11 and 12 into the aminocyclohexadiene 15 (Scheme 3). Osmate catalyzed cis-dihydroxylation of the derived bis-Boc derivative 20 (Scheme 4) Zed stereospecifically to the alpha-cis-diol 21 which was transformed into (+/-)-conduramine A-1 (27a) and its tetraacetyl derivative 27b via the epoxy compound 24. On the other hand, peracid oxidation of the diene 15 gave the beta-epoxide 28 (Scheme 5) which was cleaved to the trans-diol 29 with aqueous sulfuric acid. This diol was converted into (+/-)-conduramine F-1(34a) and its tetraacetyl derivative (34b) by a reaction sequence similar to that used for the other conduramine syntheses. Fractional crystallization of the diastereomeric mixture of Michael adducts obtained from (+/-)-3c and (-)methyl lactate gave (-)-44a and (-)-45a both in greater than or equal to 47% yield (Scheme 8). Both the carboxylic acid (+)-44b and the primary alcohol (+)-46 derived from (-)-44a were converted into (-)-3c with excess methylmagnesium bromide (ca. 40% overall yield). In the same way (-)-45a was transformed into optically pure (+)-3c. (-)-3c and (+)-3c were then converted into (-)-conduramine C-l [(-)-39a] and (+)-conduramine D-l [(+)-43a] by procedures identical to those used for the racemic compounds.

  DOI：

  10.1021/jo971907r