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(4aS,5R,8aS)-5-Methyl-2,3,4a,5,6,7,8,8a-octahydro-2(1H)-quinolinone | 140146-95-8

中文名称
——
中文别名
——
英文名称
(4aS,5R,8aS)-5-Methyl-2,3,4a,5,6,7,8,8a-octahydro-2(1H)-quinolinone
英文别名
(4aS,5R,8aS)-5-methyloctahydroquinolin-2-one;(4aS,5R)-5-methyl-2-oxodecahydroquinoline;(4aS,5R,8aS)-5-methyl-3,4,4a,5,6,7,8,8a-octahydro-1H-quinolin-2-one
(4aS,5R,8aS)-5-Methyl-2,3,4a,5,6,7,8,8a-octahydro-2(1H)-quinolinone化学式
CAS
140146-95-8
化学式
C10H17NO
mdl
——
分子量
167.251
InChiKey
MKUNLMNBVAYBDH-VGMNWLOBSA-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):
    1.7
  • 重原子数:
    12.0
  • 可旋转键数:
    0.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    29.1
  • 氢给体数:
    1.0
  • 氢受体数:
    1.0

反应信息

点击查看最新优质反应信息

文献信息

  • Stereoselective Syntheses of (+)-2-<i>epi</i>-Deoxoprosopinine, (−)-Deoxoprosophylline, (+)-<i>cis</i>-195A, and 2,5-Di-<i>epi</i>-<i>cis</i>-195A from a Common Chiral Nonracemic Building Block
    作者:Krishna Annadi、Andrew G. H. Wee
    DOI:10.1021/acs.joc.5b00621
    日期:2015.5.15
    Approaches toward the syntheses of alkaloids belonging to the 2,6-disubstituted 3-hydroxypiperidine and cis-decahydroquinoline (cis-DHQ) classes of alkaloids are developed, starting from a common chiral nonracemic bicyclic lactam lactone (BLL). Two key δ-lactam intermediates, (5S,6S)-5-hydroxy-6-hydroxymethyl- and (5S,6S)-5-hydroxy-6-methylpiperidin-2-ones, are prepared; the latter δ-lactam is obtained
    从常见的手性非外消旋双环内酰胺内酯(BLL)开始,开发了合成属于2,6-二取代的3-羟基哌啶和顺式-十氢喹啉(顺式-DHQ)类生物碱生物碱的方法。制备了两个关键的δ-内酰胺中间体,(5 S,6 S)-5-羟基-6-羟甲基-和(5 S,6 S)-5-羟基-6-甲基哌啶-2-酮。后者的δ-内酰胺是通过双环内酰胺内酯直接脱羰而获得的。BLL还用于制备(4a R,5 R,8a S)-和(4a R,5 S,8a S)-5-甲基八氢喹啉-2-酮,其涉及6 - exo - trig自由基共轭加成反应。发现在自由基环化步骤中观察到的立体选择性受烯丙基1,2-菌株的影响,该烯丙基1,2-菌株是由N-(对甲氧基苄基)基团与自由基中间体的内酰胺环中的C6取代基的相互作用引起的。2- -发达方法的有效性是通过的不对称合成(+)证实外延( - ) - -deoxoprosopinine,deoxoprosophylline,(+)
  • Removal of the Chiral Inductor from Phenylglycinol-derived Tricyclic Lactams. Unexpected Generation of Chiral trans-Hydrochromene Lactones
    作者:Rosa Griera、Alexandre Pinto、Robert Fabregat、Eric Cots、Joan Bosch、Mercedes Amat
    DOI:10.2174/1570178615666171213143657
    日期:2018.4.12
    In the search for synthetic routes for the preparation of cis- and trans- decahydroquinolin-2- ones, a procedure for the generation of enantiopure trans-hydrochromene lactones, by treatment of (R)- phenylglycinol-derived oxazoloquinolone lactams with Na/liq. NH3 followed by acidification, has been developed.
    在寻找制备顺式和反式十氢喹啉-2-的合成路线的过程中,开发了一种生成对映体纯反氢苯并喃内酯的程序,该程序是用 Na/liq.NH3处理(R)-苯基甘醇衍生的噁唑喹啉内酯,然后酸化。NH3,然后进行酸化。
  • Ruthenium-catalyzed hydration of nitriles and transformation of .delta.-keto nitriles to ene-lactams
    作者:Shunichi Murahashi、Shigehiro Sasao、Eiichiro Saito、Takeshi Naota
    DOI:10.1021/jo00035a003
    日期:1992.4
    Hydration of nitriles and transformation of delta-keto nitriles to ene-lactams can be performed efficiently by using RuH2(PPh3)4 catalyst under mild conditions. The effectiveness of the reaction is illustrated by the short-step synthesis of (-)-pumiliotoxin C.
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同类化合物

锯齿石松宁 脱氧卡色素B 箭毒蛙毒素 C 环戊二烯并[b]吖庚英-5-醇,十氢- 坎库碘铵 十氢喹啉 十氢-2-甲基喹啉 八氢对苯二酚-4(1H)-酮 八氢喹啉-2(1H)-酮 八氢-2,6-喹啉二酮 二氯化硅2,3-萘醛菁 β-羟基丙基-环糊精 [(4aS,4bR,6aS,8S,10aS,10bS,12aS)-10a,12a-二甲基-1,2,3,4,4a,4b,5,6,6a,7,8,9,10,10b,11,12-十六氢萘并[6,5-f]喹啉-8-基]2-[4-[二(2-氯乙基)氨基]苯基]乙酸酯 [(4aS,4bR,6aS,8S,10aS,10bS,12aS)-1,10a,12a-三甲基-2-氧代-3,4,4a,4b,5,6,6a,7,8,9,10,10b,11,12-十四氢萘并[6,5-f]喹啉-8-基]2-[4-[二(2-氯乙基)氨基]苯基]乙酸酯 8H-13,3,6a-乙基亚基-7,10-亚甲基噁庚并[3,4-i]-1-苯并吖辛因-8-酮,1-乙基十四氢-12a-羟基-6-甲氧基-3-甲基-,(3R,6S,6aS,7R,7aS,10S,12aS,13S,13aR,15R)-(9CI) 8-羟基-十氢喹啉 4-乙炔基-2-甲基十氢喹啉-4-醇 4-乙炔基-2-甲基-1-(3-苯丙-2-炔-1-基)十氢喹啉-4-醇 3-羟基-13,17-开环-5-雄甾烯-17-酸-13,17-内酰胺(4-(二(2-氯乙基)氨基)苯基)丁酸酯 3-甲氧基-17-氮杂-高雄甾-5-烯-17-酮 2H-环戊二烯并[b]吡啶-2-酮,八氢-4-甲基-,[4S-(4-α-,4a-bta-,7a-bta-)]-(9CI) 2-甲基-1-(3-丙氧基-丙基)-八氢-喹啉-4-酮 2,5-二丙基十氢喹啉 1-(3-甲氧基-丙基)-2-甲基-八氢-喹啉-4-酮 1-(3-氯-丙基)-十氢-喹啉 1-(3-乙氧基-丙基)-2-甲基-十氢-喹啉 1-(3-乙氧基-丙基)-2-甲基-八氢-喹啉-4-酮 1,2,2-三甲基-八氢-喹啉-4-酮 (4aS,4bR,8S,10aR,10bS,12aS)-10a,12a-二甲基-2-羰基-1,2,3,4,4a,4b,5,7,8,9,10,10a,10b,11,12,12a-十六氢萘并[2,1-f]喹啉-8-基{4-[二(2-氯乙基)氨基]苯基}乙酸酯 (4aS,4bR,6aS,8S,10aS,10bS,12aS)-8-羟基-10a,12a-二甲基-3,4,4a,4b,5,6,6a,7,8,9,10,10b,11,12-十四氢-1H-萘并[2,1-f]喹啉-2-酮 (3S,13R)-1,2,3,4,4aalpha,5,11,11aalpha-八氢-2,2,5-三甲基-3beta,5beta-乙桥-10bH-吡啶并[3,2-b]咔唑-10bbeta,13-二醇 (3R,6S,6aS,7R,7aS,10S,12aS,13R,13aR,14S,15R)-1-乙基十四氢-12a,14-二羟基-6-甲氧基-3-甲基-8H-13,3,6a-亚乙基-7,10-甲桥氧杂卓并[3,4-i]-1-苯并氮杂环辛四烯-8-酮 (2S,4aR,8aR)-2-甲基八氢-4(1H)-喹啉酮 (2R,4R,4As,8As)-rel-4-乙炔基十氢-1,2-二甲基-4-喹啉醇 1-(2-Cyclopentylethyl)-perhydrochinolin Perhydrodibenzochinolizin octahydroquinoline-1(2H)-carbonitrile N-Acetylbaikeidin 4-[4-[(4aR,8aR)-3,4,4a,5,6,7,8,8a-octahydro-2H-quinoline-1-carbonyl]thiophen-2-yl]piperidine-1-carboxamide N-Chlor-trans-decahydrochinolin (4aR,8aR)-1-{4-[4-(octahydro-quinoline-1(2H)-ylcarbonyl)-thiophen-2-yl]-piperidin-1-yl}-ethanone (7-Acetyl-3a,6-dimethyl-3-oxo-tetradecahydro-7-aza-cyclohepta[e]inden-6-yl)-acetic acid 6,7-Cyclobutano-1,2-cyclopropano-chinolizidin 2-Methyl-2,3-tetramethylen-N-cyanoaziridin (4aR)-2-oxo-1-[(1R)-1-phenylethyl]-4,5,6,7-tetrahydro-3H-quinoline-4a-carboxylic acid (4aR,8aR)-(octahydro-quinolin-1(2H)-yl)-(5-piperidin-4-yl-thiophen-3-yl)-methanone 5-(octahydroquinolin-1-yl)-5-oxopentanoic acid N-benzyl-N-isopropylamide 3,4,4-Trimethyl-2-azabicyclo<3.3.0>octan (4aR,8aR)-4-[4-(octahydro-quinoline-1(2H)-ylcarbonyl)-thiophen-2-yl]-piperidine-1-carboxylic acid tert-butyl ester 1-Aza-4,11-dioxo-3-oxo-methoxycarbonyl-tricyclo<5.3.1.05,10>undecan