(1S,4S,5R)-N-(Benzyloxycarbonyl)-4-(methoxymethyl)-3-oxa-6-azabicyclo<3.1.0>hexan-2-one | 162895-89-8

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (1S,4S,5R)-N-(Benzyloxycarbonyl)-4-(methoxymethyl)-3-oxa-6-azabicyclo<3.1.0>hexan-2-one
• 英文别名: benzyl (1R,2S,5S)-2-(methoxymethyl)-4-oxo-3-oxa-6-azabicyclo[3.1.0]hexane-6-carboxylate
• CAS: 162895-89-8
• 化学式: C₁₄H₁₅NO₅
• 分子量: 277.277
• InChiKey: WJIURWUMIOCQKQ-ATUXAFSHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  64.8
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (1S,4S,5R)-N-(Benzyloxycarbonyl)-4-(methoxymethyl)-3-oxa-6-azabicyclo<3.1.0>hexan-2-one 在 三氟化硼乙醚 、 lithium bromide 作用下， 以 氯仿 为溶剂， 反应 4.0h， 以80%的产率得到3--2-bromo-2,3-dideoxy-5-O-methyl-D-xylono-1,4-lactone
  参考文献：
  名称：

  Reactivity of 2,3-Aziridino-2,3-dideoxy-D-lyxono-.gamma.-lactone Derivatives, Rigid Analogs of Aziridine-2-carboxylic Esters, toward Soft and Hard Nucleophiles: Control of Lactone vs Aziridine Ring Opening and C-2 vs C-3 Regioselectivity

  摘要：

  The reactivities of (1S,4S,5R)-N-acetyl-4-(methoxymethyl)-3-oxa-6-azabicyclo[3.1.0]hexan-2-one (2) and its N-Cbz analogue 12 toward soft nucleophiles (thiols, acetic acid, bromide) and hard nucleophiles (alcohols, benzylamine) were studied and compared to the reported reactivities of aziridine-2-carboxylic esters (1) with the same nucleophiles. Both 2 and 12 reacted with soft nucleophiles in the presence of a Lewis acid to give the products of aziridine ring opening at C-2. This regioselectivity is in distinct contrast to the known reactions of 1 with these nucleophiles wherein aziridine ring opening at C-3 is almost always observed. The Lewis acid-catalyzed reaction of 2 with alcohols (methanol or benzyl alcohol) gave products arising from initial attack of the lactone ring yielding the corresponding methyl or benzyl esters, respectively. These intermediates further reacted to give, in the case of methanol, exclusively the product of N-deacetylation, that is, aziridine-2-carboxylic methyl ester 20 or, in the case of benzyl alcohol, a mixture of the N-deacetylated aziridine-2-carboxylic benzyl esters 17 and 18, the results of both lactone ring opening and aziridine ring opening at C-3. The latter compound spontaneously cyclized to its lactone form 19 during the course of its purification. N-Deacetylation by alcohols could be suppressed by using the N-Cbz aziridine derivative 12 as starting material. Thus, 12 reacted with methanol or benzyl alcohol in the presence of a Lewis acid to give lactones 21 and 22, respectively, the products of aziridine ring opening at C-3. The intermediacy of an aziridine-2-carboxylic ester derivative in these reactions, via initial opening of the lactone ring by the alcohol, was demonstrated by the isolation of the isopropyl ester 24 when 12 was treated with isopropyl alcohol. The reactions of 2 and 12 with benzylamine in the absence of Lewis acid catalysis paralleled those with alcohols. Thus, 2 gave aziridine-2-carboxamide 25, the product of lactone ring opening and N-deacetylation while the N-Cbz aziridine 12 yielded only the product of lactone ring opening, benzylamide 27. As predicted by perturbational and HSAB (hard and soft acids and bases) theories, the regioselectivity of attack of 2 and 12 by soft nucleophiles is directed toward the center having the highest LUMO coefficient (C-2) (determined using MNDO calculations) while hard nucleophiles react with centers having the highest charge (C-1, C-1'). The synthetic potential of 2,3-aziridino gamma-lactones of types 2 and 12, as compared to the classical aziridine-2-carboxylic esters, is discussed in terms of these results.

  DOI：

  10.1021/jo00112a027
• 作为产物：
  描述：

  N-(Benzyloxycarbonyl)-2,3-aziridino-2,3-dideoxy-5-O-methyl-α,β-D-lyxofuranose 在 N-甲基吲哚酮 、 四丙基高钌酸铵 、 4 A molecular sieve 作用下， 以 乙腈 为溶剂， 反应 5.0h， 以75%的产率得到(1S,4S,5R)-N-(Benzyloxycarbonyl)-4-(methoxymethyl)-3-oxa-6-azabicyclo<3.1.0>hexan-2-one
  参考文献：
  名称：

  Reactivity of 2,3-Aziridino-2,3-dideoxy-D-lyxono-.gamma.-lactone Derivatives, Rigid Analogs of Aziridine-2-carboxylic Esters, toward Soft and Hard Nucleophiles: Control of Lactone vs Aziridine Ring Opening and C-2 vs C-3 Regioselectivity

  摘要：

  The reactivities of (1S,4S,5R)-N-acetyl-4-(methoxymethyl)-3-oxa-6-azabicyclo[3.1.0]hexan-2-one (2) and its N-Cbz analogue 12 toward soft nucleophiles (thiols, acetic acid, bromide) and hard nucleophiles (alcohols, benzylamine) were studied and compared to the reported reactivities of aziridine-2-carboxylic esters (1) with the same nucleophiles. Both 2 and 12 reacted with soft nucleophiles in the presence of a Lewis acid to give the products of aziridine ring opening at C-2. This regioselectivity is in distinct contrast to the known reactions of 1 with these nucleophiles wherein aziridine ring opening at C-3 is almost always observed. The Lewis acid-catalyzed reaction of 2 with alcohols (methanol or benzyl alcohol) gave products arising from initial attack of the lactone ring yielding the corresponding methyl or benzyl esters, respectively. These intermediates further reacted to give, in the case of methanol, exclusively the product of N-deacetylation, that is, aziridine-2-carboxylic methyl ester 20 or, in the case of benzyl alcohol, a mixture of the N-deacetylated aziridine-2-carboxylic benzyl esters 17 and 18, the results of both lactone ring opening and aziridine ring opening at C-3. The latter compound spontaneously cyclized to its lactone form 19 during the course of its purification. N-Deacetylation by alcohols could be suppressed by using the N-Cbz aziridine derivative 12 as starting material. Thus, 12 reacted with methanol or benzyl alcohol in the presence of a Lewis acid to give lactones 21 and 22, respectively, the products of aziridine ring opening at C-3. The intermediacy of an aziridine-2-carboxylic ester derivative in these reactions, via initial opening of the lactone ring by the alcohol, was demonstrated by the isolation of the isopropyl ester 24 when 12 was treated with isopropyl alcohol. The reactions of 2 and 12 with benzylamine in the absence of Lewis acid catalysis paralleled those with alcohols. Thus, 2 gave aziridine-2-carboxamide 25, the product of lactone ring opening and N-deacetylation while the N-Cbz aziridine 12 yielded only the product of lactone ring opening, benzylamide 27. As predicted by perturbational and HSAB (hard and soft acids and bases) theories, the regioselectivity of attack of 2 and 12 by soft nucleophiles is directed toward the center having the highest LUMO coefficient (C-2) (determined using MNDO calculations) while hard nucleophiles react with centers having the highest charge (C-1, C-1'). The synthetic potential of 2,3-aziridino gamma-lactones of types 2 and 12, as compared to the classical aziridine-2-carboxylic esters, is discussed in terms of these results.

  DOI：

  10.1021/jo00112a027