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N-甲基吗啉氧化物 → 2-(2,3-Dihydroxypropyl)-5-[4-(1H-pyrazol-1-yl)benzyl]-2,5-dihydro-3H-pyrazolo[4,3-c]cinnolin-3-one

HRID 241978
笔记
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反应方程式

HRID 241978 反应方程式
[CH2:1]([N:4]1[C:28](=[O:29])[C:7]2=[N:8][N:9]([CH2:16][C:17]3[CH:22]=[CH:21][C:20]([N:23]4[CH:27]=[CH:26][CH:25]=[N:24]4)=[CH:19][CH:18]=3)[C:10]3[CH:11]=[CH:12][CH:13]=[CH:14][C:15]=3[C:6]2=[N:5]1)[CH:2]=C.C[N+]1([O-])CC[O:34]CC1.[C:38](=[O:41])(O)[O-].[Na+]>O1CCCC1.O.[Os](=O)(=O)(=O)=O>[OH:34][CH:2]([CH2:38][OH:41])[CH2:1][N:4]1[C:28](=[O:29])[C:7]2=[N:8][N:9]([CH2:16][C:17]3[CH:18]=[CH:19][C:20]([N:23]4[CH:27]=[CH:26][CH:25]=[N:24]4)=[CH:21][CH:22]=3)[C:10]3[CH:11]=[CH:12][CH:13]=[CH:14][C:15]=3[C:6]2=[N:5]1
参与物实验过程后处理来源与证据反应笔记

参与物

7

反应物 3

HCID 82029N-甲基吗啉氧化物HCID 516892碳酸氢钠HCID 46897482Allyl-5-[4-(1H-pyrazol-1-yl)benzyl]-2,5-dihydro-3H-pyrazolo[4,3-c]cinnolin-3-one

产物 1

HCID 468965082-(2,3-Dihydroxypropyl)-5-[4-(1H-pyrazol-1-yl)benzyl]-2,5-dihydro-3H-pyrazolo[4,3-c]cinnolin-3-one

试剂、催化剂与溶剂 3

HCID 30318锇酸催化剂
HCID 962
聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]
溶剂
HCID 8028四氢呋喃溶剂

实验过程

Allyl-5-[4-(1H-pyrazol-1-yl)benzyl]-2,5-dihydro-3H-pyrazolo[4,3-c]cinnolin-3-one [(Example 10), 600 mg, 1.57 mmol] was dissolved in tetrahydrofuran (65 mL) and water (65 mL), treated with 4-methylmorpholine 4-oxide (221 mg, 1.88 mmol, 1.2 equiv) and osmium tetroxide (50.0 μL, 0.160 mmol, 0.1 equiv). The mixture was stirred for 72 hours at ambient temperature, poured into sodium bicarbonate (200 mL, saturated aqueous) and extracted with ethyl acetate (2×150 mL) and chloroform (2×100 mL). The combined organic extracts were dried with sodium sulfate, filtered and concentrated in vacuo. The sodium sulfate was washed with a 1:1 mixture of methanol:chloroform (6×30 mL) and the filtrate was concentrated in vacuo. The residue was purified via silica gel gradient chromatography (100:0 to 85:15; dichloromethane:methanol), providing the titled compound: 1H-NMR (400 MHz, CDCl3) δ 8.30-8.26 (1H, m), 7.89 (1H, d, J=2.5 Hz), 7.72-7.67 (3H, m), 7.62-7.54 (3H, m), 7.39 (2H, d, J=8.4 Hz), 6.47-6.45 (1H, m), 5.88 (2H, s), 4.31 (2H, dd, J=5.3, 2.0 Hz), 4.18-4.13 (1H, m), 3.69-3.65 (2H, m), 3.49 (1H, d, J=5.8 Hz), 3.02 (1H, m); high resolution mass spectrometry (ES+) m/z 417.1684 [(M+H)+; calculated for C22H21N6O3: 417.1670].

后处理

  1. extractionextracted with ethyl acetate (2×150 mL) and chloroform (2×100 mL)
  2. dry with materialThe combined organic extracts were dried with sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. washThe sodium sulfate was washed with a 1:1 mixture of methanol
  6. concentrationchloroform (6×30 mL) and the filtrate was concentrated in vacuo
  7. customThe residue was purified via silica gel gradient chromatography (100:0 to 85:15; dichloromethane:methanol)

来源与证据

ORD记录
ord-cb17d77449c143ad86538ad964216021
来源数据集
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08653079B2

反应笔记

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本页导航参与物实验过程后处理来源与证据反应笔记