Water → HCID 66834455、化合物

HRID 2275133

反応式

HRID 2275133 の反応式
[CH2:1]([N:3]([CH2:29][CH3:30])[CH2:4][CH2:5][S:6][C:7]1[CH:8]=[CH:9][C:10]2[C:22](=[O:23])[C:21]3[C:20]4[C:15](=[CH:16][C:17]([C:24]#[N:25])=[CH:18][CH:19]=4)[NH:14][C:13]=3[C:12]([CH3:27])([CH3:26])[C:11]=2[CH:28]=1)[CH3:2].[OH:31]OS([O-])=O.[K+].[OH2:37]>CO>[CH2:29]([N:3]([CH2:1][CH3:2])[CH2:4][CH2:5][S:6]([C:7]1[CH:8]=[CH:9][C:10]2[C:22](=[O:23])[C:21]3[C:20]4[C:15](=[CH:16][C:17]([C:24]#[N:25])=[CH:18][CH:19]=4)[NH:14][C:13]=3[C:12]([CH3:26])([CH3:27])[C:11]=2[CH:28]=1)(=[O:31])=[O:37])[CH3:30]

参加物

5

反応物 3

HCID 962WaterHCID 23707502Potassium hydroxy sulfiteHCID 668339748-(2-Diethylamino-ethylsulfanyl)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile

生成物 1

HCID 66834455HCID 66834455、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

8-(2-Diethylamino-ethylsulfanyl)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile (Compound B2-17, 16.8 mg, 0.0402 mmol) was dissolved in methanol (1.5 mL), added with oxone (54.3 mg, 2.2 eq.) which had been dissolved in water (0.5 mL), and then stirred at room temperature for 2 hr. The reaction solution was concentrated, extracted with ethyl acetate, washed with saturated sodium hydrogen carbonate, and dried over magnesium sulfate. The drying agent was removed by filtration and the residues obtained after concentration under reduced pressure were purified by silica gel column chromatography (dichloromethane/methanol) to obtain the target compound (white solid, 5.8 mg, 32%).

後処理

  1. concentrationThe reaction solution was concentrated
  2. extractionextracted with ethyl acetate
  3. washwashed with saturated sodium hydrogen carbonate
  4. dry with materialdried over magnesium sulfate
  5. customThe drying agent was removed by filtration
  6. customthe residues obtained
  7. concentrationafter concentration under reduced pressure
  8. customwere purified by silica gel column chromatography (dichloromethane/methanol)
  9. customto obtain the target compound (white solid, 5.8 mg, 32%)

出典と根拠

ORDレコード
ord-83e01f0eb8e544b4aa32e1a7f13544fb
出典データセット
uspto-grants-2015_09
特許番号
US09126931B2

関連ノート

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