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Tetrahydrofuran → 8-(1,2-Dihydroxy-ethyl)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile

HRID 61759
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HRID 61759 반응식
[CH2:1]1[CH2:5][O:4][CH2:3][CH2:2]1.[CH3:6][C:7]1([CH3:29])[C:19]2[NH:18][C:17]3[C:12](=[CH:13][CH:14]=[C:15]([C:20]#[N:21])[CH:16]=3)[C:11]=2[C:10](=[O:22])[C:9]2[CH:23]=[CH:24]C(C=C)=C[C:8]1=2.C[N+]1([O-])CC[O:34]CC1.C(N(CC(O)=O)CC(O)=O)CN(CC(O)=O)CC(O)=O.[Na].[Na]>[Os](=O)(=O)(=O)=O.C(O)(C)(C)C>[OH:34][CH:1]([C:2]1[CH:24]=[CH:23][C:9]2[C:10](=[O:22])[C:11]3[C:12]4[C:17](=[CH:16][C:15]([C:20]#[N:21])=[CH:14][CH:13]=4)[NH:18][C:19]=3[C:7]([CH3:6])([CH3:29])[C:8]=2[CH:3]=1)[CH2:5][OH:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 8028TetrahydrofuranHCID 82029Methyl morpholine oxideHCID 9949814Ethylenediaminetetraacetic acid disodiumHCID 668340546,6-Dimethyl-11-oxo-8-vinyl-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile

생성물 1

HCID 668343198-(1,2-Dihydroxy-ethyl)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile수율 63%

시약·촉매·용매

2
HCID 30318Osmium Tetroxide촉매HCID 6386tert-Butanol용매

실험 절차

To the THF (1 ml) solution of 6,6-dimethyl-11-oxo-8-vinyl-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile (Compound B2-24, 20 mg, 0.064 mmol), t-butanol solution of osmium tetraoxide (19 μl, 0.3 eq.) and 50% aqueous solution of N-methylmorpholine-N-oxide (30 μl, 2.0 eq.) were added and the mixture was stirred at room temperature for 3 hr. To the reaction solution, 10% aqueous solution of disodium ethylenediamine tetraacetic acid was added, followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate. The drying agent was removed by filtration and the residues obtained after concentration under reduced pressure were purified by high performance liquid chromatography to obtain the title compound (21 mg, 63%).

후처리

  1. extractionfollowed by extraction with ethyl acetate
  2. dry with materialThe organic layer was dried over sodium sulfate
  3. customThe drying agent was removed by filtration
  4. customthe residues obtained
  5. concentrationafter concentration under reduced pressure
  6. customwere purified by high performance liquid chromatography

출처 및 근거

ORD 기록
ord-03b2809b6fa64788afce4cfbaaeacb88
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09440922B2

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