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7-benzyl-8a-methoxy-7-methyl-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-on | 133712-70-6

中文名称
——
中文别名
——
英文名称
7-benzyl-8a-methoxy-7-methyl-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-on
英文别名
4-Benzyl-8a-methoxy-7-methyl-2,3-dihydro-1,4-benzoxazin-6-one
7-benzyl-8a-methoxy-7-methyl-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-on化学式
CAS
133712-70-6
化学式
C17H19NO3
mdl
——
分子量
285.343
InChiKey
RQZHTBUVJLHMJH-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):
    1.8
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    38.8
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    重氮乙烷7-benzyl-8a-methoxy-7-methyl-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-on氯仿 为溶剂, 反应 3.0h, 以80%的产率得到(6aR,9aS,9bS)-4-benzyl-9b-methoxy-6a,9-dimethyl-2,3,9,9a-tetrahydropyrazolo[3,4-h][1,4]benzoxazin-6-one
    参考文献:
    名称:
    Zur Umsetzung von 3,4-Dihydro-8a-methoxy-2H-1,4-benzoxazin-6(8aH)-onen mit Diazoalkanen, 1. Mitt.
    摘要:
    3,4-Dihydro-8a-methoxy-2H-1,4-benzoxazin-6(8a')-ones - quinol derivatives of 2-hydroxyethylamino-1, 4-benzoquinones - react with diazoalkanes to yield 2,3,9a,9b-Tetrahydro-9H-pyrazolo[3,4-h]-1, 4-benzoxazin-6(6 aH)-ones (3). Their structures were established on basis of NMR-techniques including two-dimensional experiments. The orientation phenomena of the reaction is discussed.
    DOI:
    10.1007/bf00815165
  • 作为产物:
    描述:
    4-Benzyl-8a-hydroxy-7-methyl-3,4-dihydro-2H,8aH-benzo[1,4]oxazin-6-one碘甲烷silver(l) oxide 作用下, 以 丙酮 为溶剂, 反应 12.0h, 以47%的产率得到7-benzyl-8a-methoxy-7-methyl-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-on
    参考文献:
    名称:
    Zur Umsetzung von 3,4-Dihydro-8a-methoxy-2H-1,4-benzoxazin-6(8aH)-onen mit Diazoalkanen, 1. Mitt.
    摘要:
    3,4-Dihydro-8a-methoxy-2H-1,4-benzoxazin-6(8a')-ones - quinol derivatives of 2-hydroxyethylamino-1, 4-benzoquinones - react with diazoalkanes to yield 2,3,9a,9b-Tetrahydro-9H-pyrazolo[3,4-h]-1, 4-benzoxazin-6(6 aH)-ones (3). Their structures were established on basis of NMR-techniques including two-dimensional experiments. The orientation phenomena of the reaction is discussed.
    DOI:
    10.1007/bf00815165
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文献信息

  • Reactions of 2H-3,4-dihydro-1,4-benzoxazin-6(8aH)-ones with 2,4,6-trimethylbenzonitrile oxide, III
    作者:M. Schubert-Zsilavecz、D. Gusterhuber、W. Likussar、G. F�rber
    DOI:10.1007/bf01277634
    日期:1994.6
    Regio-, stereo- and siteselectivity of the cycloadditions of trimethylbenzonitrile oxide with 2H-3,4-Dihydro-1,4-benzoxazin-6(8aH)-ones have been investigated. The structures of the obtained products were elucidated by means of homonuclear NOE difference spectroscopy and HMQC and HMBC spectra. The structure of 6-Benzyl-9a-methoxy-3-mesityl-9b-methyl-7,8,9a,9b-tetrahydro-3aH-1,2-oxazolo-[4,5-h]1,4-benzoxazin-4(6H)-on 5 was elucidated from a single crystal X-ray structure analysis at ambient temperature: C27H30N2O4, M=446.55 g/mol, monoclinic, P2(1)/c, a = 10.372 (34) angstrom, b = 11.908 (21) angstrom, c = 20.040 (34) angstrom, beta = 97.16 (17)-degrees, V = 2455.8 (1.9) angstrom3, Z = 4, d(c) = 1.208 g/cm3, mu = 0.08 mm-1, R = 0.0546.
  • SCHUBERT-ZSILAVECZ, MANFRED, MONATSH. CHEM., 122,(1991) N-2, C. 51-57
    作者:SCHUBERT-ZSILAVECZ, MANFRED
    DOI:——
    日期:——
  • Schubert-Zsilavecz M., Gusterhuber D., Likussar W., Faerber G., Monatsh. Chem, 125 (1994) N 6-7, S 735-742
    作者:Schubert-Zsilavecz M., Gusterhuber D., Likussar W., Faerber G.
    DOI:——
    日期:——
  • Zur Umsetzung von 3,4-Dihydro-8a-methoxy-2H-1,4-benzoxazin-6(8aH)-onen mit Diazoalkanen, 1. Mitt.
    作者:Manfred Schubert-Zsilavecz
    DOI:10.1007/bf00815165
    日期:——
    3,4-Dihydro-8a-methoxy-2H-1,4-benzoxazin-6(8a')-ones - quinol derivatives of 2-hydroxyethylamino-1, 4-benzoquinones - react with diazoalkanes to yield 2,3,9a,9b-Tetrahydro-9H-pyrazolo[3,4-h]-1, 4-benzoxazin-6(6 aH)-ones (3). Their structures were established on basis of NMR-techniques including two-dimensional experiments. The orientation phenomena of the reaction is discussed.
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