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5-Carbomethoxy-2-N-tert-butyloxycarbonyl-2-aminomethyl-5H-6-oxo-2,3,4,4a,7,7a-hexahydropyrano<2,3-b>furan | 133786-82-0

中文名称
——
中文别名
——
英文名称
5-Carbomethoxy-2-N-tert-butyloxycarbonyl-2-aminomethyl-5H-6-oxo-2,3,4,4a,7,7a-hexahydropyrano<2,3-b>furan
英文别名
methyl 6-[[(2-methylpropan-2-yl)oxycarbonylamino]methyl]-2-oxo-3,3a,4,5,6,7a-hexahydrofuro[2,3-b]pyran-3-carboxylate
5-Carbomethoxy-2-N-tert-butyloxycarbonyl-2-aminomethyl-5H-6-oxo-2,3,4,4a,7,7a-hexahydropyrano<2,3-b>furan化学式
CAS
133786-82-0
化学式
C15H23NO7
mdl
——
分子量
329.35
InChiKey
PLDPKXWTQWIYIB-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):
    0.98
  • 重原子数:
    23.0
  • 可旋转键数:
    3.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    100.16
  • 氢给体数:
    1.0
  • 氢受体数:
    7.0

反应信息

  • 作为反应物:
    描述:
    5-Carbomethoxy-2-N-tert-butyloxycarbonyl-2-aminomethyl-5H-6-oxo-2,3,4,4a,7,7a-hexahydropyrano<2,3-b>furanlithium chloride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 12.0h, 以57%的产率得到2-N-tert-Butoxycarbonyl-aminomethyl-5H-2,3,4,4a,7,7a-hexahydro-6-oxopyrano<2,3-b>furan
    参考文献:
    名称:
    乙酸锰介导的烯醇醚向γ-内酯的转化
    摘要:
    乙酸锰和带有2-取代的二氢吡喃的丙二酸甲酯钾以良好的产率提供了相应的稠合γ-内酯。具有较少酸性亚甲基质子的羧酸在该反应中失败。
    DOI:
    10.1016/s0040-4039(00)74474-1
  • 作为产物:
    描述:
    monomethyl monopotassium malonatetert-butyl ((3,4-dihydro-2H-pyran-2-yl)methyl)carbamate 在 manganese triacetate 、 溶剂黄146 作用下, 反应 0.17h, 以47%的产率得到5-Carbomethoxy-2-N-tert-butyloxycarbonyl-2-aminomethyl-5H-6-oxo-2,3,4,4a,7,7a-hexahydropyrano<2,3-b>furan
    参考文献:
    名称:
    乙酸锰介导的烯醇醚向γ-内酯的转化
    摘要:
    乙酸锰和带有2-取代的二氢吡喃的丙二酸甲酯钾以良好的产率提供了相应的稠合γ-内酯。具有较少酸性亚甲基质子的羧酸在该反应中失败。
    DOI:
    10.1016/s0040-4039(00)74474-1
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文献信息

  • Manganic acetate mediated transformation of enol-ethers into gamma-lactones
    作者:Michelle del Rosario-Chow、Jiraporn Ungwitayatorn、Bruce L. Currie
    DOI:10.1016/s0040-4039(00)74474-1
    日期:1991.2
    Manganic acetate and potassium methyl malonate with a 2-substituted dihydropyran provide the corresponding fused gamma-lactone in good yield. Carboxylic acids with less acidic methylene protons fail in this reaction.
    乙酸锰和带有2-取代的二氢吡喃的丙二酸甲酯钾以良好的产率提供了相应的稠合γ-内酯。具有较少酸性亚甲基质子的羧酸在该反应中失败。
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同类化合物

马桑宁内酯 苦毒浆果[木防已属] 苦亭 艾瑞布林中间体 艾瑞布林 甲磺酸艾日布林 木防己苦毒宁 全内酯 二氢苦毒宁 6-甲基-4-氧代-4H-呋喃并[3,2-c]吡喃-3-甲酰氯 6-(4-羟基苯基)-2,3,3-三甲基-2H-呋喃并[5,4-b]吡喃-4-酮 4H-呋喃并[2,3-c]吡喃基莫匹罗星钠 3-甲基2H-呋喃并[2,3-c]吡喃-2-酮 3,5-二甲基2H-呋喃并[2,3-c]吡喃-2-酮 2H-呋喃并[2,3-c]吡喃-2-酮 2-[(1E,3E)-己-1,3-二烯基]-2,6-二甲基-5,6-二氢呋喃并[5,4-b]吡喃-3,4-二酮 (3aS,5S,6R,9E,14R,15R,15aR)-2,3,3a,4,5,6,7,8,11,12,13,14,15,15alpha-十四氢-6,10,14-三甲基-3-亚甲基-2-氧代-5,15-环氧环十四烷并[b]呋喃-6-醇乙酸酯 (3aR,4S,7aR)-4-羟基-3,3a,4,7a-四氢呋喃并[5,4-b]吡喃-2-酮 5-hydroxymethyl-3-methyl-2H-furo[2,3-c]pyran-2-one 5-fluoromethyl-2H-furo[2,3-c]pyran-2-one 5-chloromethyl-2H-furo[2,3-c]pyran-2-one 10,11-Anhydro-5-deoxy-1,2-O-isopropylidene-9-O-(methoxymethyl)-β-L-xylo-L-ido-7-undeculofuranose-(1,4)-pyranose-(7,3) 3,7-dimethyl-2H-furo[2,3-c]pyran-2-one 4R-(3αβ,3aβ,4β,5α,6β,7aβ)hexahydro-2,2-dimethyl-4,5-bis(phenylmethoxy)-6-[(phenylmethoxy)methyl]4H-furo[2,3-b]pyran-3-ol 10,10-dimethyl-5-(methylsulfanyl)-10,11-dihydro-8H-pyrano[4',3':4,5]furo[3,2-e]tetrazolo[1,5-c]pyrimidine (R)-3-((2R,3R,5aR,7R,9aS)-3-hydroxyhexahydro-2H-2,5a-methanopyrano[3,2-e][1,4]dioxepin-7-yl)-2-methylpropanenitrile 13-methyl-8,10,12-trioxapentacyclo[5.5.2.02,6.O3,11.05,9]-13-tetradecene 2,3,4,4a,7,8-Hexahydro-6H-2-(acetoxymethyl)-3,4-diacetoxy-1,9-dioxacyclohexainden-5-one 2,3,4,4a,7,8-Hexahydro-6H-2-methoxy-1,9-dioxacyclohexainden-5-one (-)-3a-methyl-3a,4-dihydro-1H,3H-furo[3,4-c]pyran-6,6,7-tricarboxylic acid 6,6-diethyl ester 7-methyl ester (+)-8-epi-altholactone 4-(perfluorophenyl)-3-phenylhexahydro-1H-furo[3,4-c]pyran [(2R,11S,12R,14R,15R,17R,19S)-19-tert-butyldiphenylsiloxymethyl-15-methyl-13,18-dioxadispiro(2H-3,6-dihydropyran-6,5'-oxolane-2',3''-bicyclo[4.3.0]nonane)-2-yl]phenylmethoxymethane (3aS,5S,9bS)-5-methyl-3,3a-dihydro-5H-furo[3,2-c]isochromene-2,6,9-(9bH)-trione (3aR,5R,7aR)-5-(2-hydroxypropan-2-yl)-7a-methylhexahydro-2H-furo[3,2-b]pyran-2-one 2,2,3b-trimethyl-7-vinyl-3a,5,7a,8a-tetrahydro-3bH-1,3,4,8-tetracyclopenta[a]indene ethyl 4-oxo-3-phenyl-3,3a,4,6-tetrahydro-1H-furo[3,4-c]pyran-3a-carboxylate methyl (2R,2aR,4aS,7aS,7bS)-2-methoxy-6-methyl-4-oxo-5-pentyl-2a,4,4a,7b-tetrahydro-2H-1,3,7-trioxacyclopenta[cd]indene-7a-carboxylate 4-nonyl-3-phenylhexahydro-1H-furo[3,4-c]pyran 3'-(4-methoxyphenyl)-7a'-methyl-4'H,6'H-spiro[cyclohexane-1,5'-furo[2,3-b]pyran]-2'(7a'H)-one 3',7a'-dimethyl-4'H,6'H-spiro[cyclohexane-1,5'-furo[2,3-b]pyran]-2'(7a'H)-one 2-(methylsulfanyl)-5,6-dihydro-4H-furo[2,3-b]pyran 1,1-(3-dimethylamino-3-phenylpentamethylen)-3,4-dihydro-1H-2,9-dioxafluoren 7-cyclopropyl-4,5,7,7a-tetrahydro-furo[2,3-c]pyran-2-one 7-cyclopropyl-3-phenyl-4,5,7,7a-tetrahydro-furo[2,3-c]pyran-2-one 7-cyclopropyl-3-phenyl-4,5,7,7a-tetrahydro-furo[2,3-c]pyran-2-one (4'R)-6-O-(4-cyanophenyl)-1,2,3,4-tetradeoxy-4'-(2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-heptadecafluorononyl)-2',3',4',5'-tetrahydro-α-D-erythro-hexopyranoso[1,2-b]furan 2,2,3,6-tetramethyl-2,3-dihydro-4H-furo[2,3-b]pyran-4-one (1aR,4aS,5R)-7-carboethoxy-5-methylethyl-tetrahydrofurano[2,3-b]3,4-dihydro-2H-pyran (3aS,4S,7aR)-ethyl 4-methyl-3,3a,4,7a-tetrahydro-2H-furo[2,3-b]pyran-6-carboxylate