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Sodium Thiosulfate → 3-(5-Isopropyl-2,4-bis-methoxymethoxyphenyl)-4-[4-(4-methylpiperazin-1-ylmethyl)phenyl]-5-methanesulfonyl-[1,2,4]triazole

HRID 1947210
ノート
印刷プレビュー

反応式

HRID 1947210 の反応式
Cl[C:2]1C=CC=C(C(OO)=O)C=1.[CH:12]([C:15]1[C:16]([O:46][CH2:47][O:48][CH3:49])=[CH:17][C:18]([O:42][CH2:43][O:44][CH3:45])=[C:19]([C:21]2[N:25]([C:26]3[CH:31]=[CH:30][C:29]([CH2:32][N:33]4[CH2:38][CH2:37][N:36]([CH3:39])[CH2:35][CH2:34]4)=[CH:28][CH:27]=3)[C:24](SC)=[N:23][N:22]=2)[CH:20]=1)([CH3:14])[CH3:13].[S:50]([O-:54])([O-])(=[O:52])=S.[Na+].[Na+].S(=O)(O)[O-].[K+].C(=O)([O-])O.[Na+]>C(OCC)C.C(Cl)Cl>[CH:12]([C:15]1[C:16]([O:46][CH2:47][O:48][CH3:49])=[CH:17][C:18]([O:42][CH2:43][O:44][CH3:45])=[C:19]([C:21]2[N:25]([C:26]3[CH:31]=[CH:30][C:29]([CH2:32][N:33]4[CH2:34][CH2:35][N:36]([CH3:39])[CH2:37][CH2:38]4)=[CH:28][CH:27]=3)[C:24]([S:50]([CH3:2])(=[O:54])=[O:52])=[N:23][N:22]=2)[CH:20]=1)([CH3:13])[CH3:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 24477Sodium ThiosulfateHCID 70297m-Chloroperbenzoic acid2 回HCID 516892Sodium BicarbonateHCID 23663620Potassium BisulfiteHCID 598299083-(5-Isopropyl-2,4-bis-methoxymethoxyphenyl)-4-[4-(4-methylpiperazin-1-ylmethyl)phenyl]-5-methylsulfanyl-[1,2,4]triazole

生成物 1

HCID 59829856
3-(5-Isopropyl-2,4-bis-methoxymethoxyphenyl)-4-[4-(4-methylpiperazin-1-ylmethyl)phenyl]-5-methanesulfonyl-[1,2,4]triazole
収率 50%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 6344Dichloromethane溶媒

実験手順

3-chloroperbenzoic acid (3.91 g, 22.7 mmol) was added to a methylene chloride (9 mL) solution of 3-(5-isopropyl-2,4-bis-methoxymethoxyphenyl)-4-[4-(4-methylpiperazin-1-ylmethyl)phenyl]-5-methylsulfanyl-[1,2,4]triazole (F652-07, 2.05 g, 3.78 mmol). After stirring at room temperature for 9.5 hours, additional 3-chloroperbenzoic acid (717 mg, 4.15 mmol) was added and stirring was continued overnight. After cooling to ice cold, saturated aqueous sodium thiosulfate and then 10% aqueous potassium bisulfite were added, and stirring was continued for a while. Further, saturated aqueous sodium hydrogencarbonate was added and the mixture was stirred, and then extracted with chloroform. The extract was washed sequentially with saturated aqueous sodium hydrogencarbonate, water and saturated sodium chloride solution, and dried over anhydrous sodium sulfate. Filtration and evaporation gave pale brown foam. After adding diethyl ether, the insoluble solids were removed by filtration, and the solvent in the filtrate was distilled off under reduced pressure. The solids thus obtained were purified by silica gel column chromatography (chloroform, methanol) to obtain 3-(5-isopropyl-2,4-bis-methoxymethoxyphenyl)-4-[4-(4-methylpiperazin-1-ylmethyl)phenyl]-5-methanesulfonyl-[1,2,4]triazole (F652-08, pale yellow foam, 1.08 g, 50%).

後処理

  1. stirringstirring
  2. waitwas continued overnight
  3. stirringstirring
  4. stirringthe mixture was stirred
  5. extractionextracted with chloroform
  6. washThe extract was washed sequentially with saturated aqueous sodium hydrogencarbonate, water and saturated sodium chloride solution
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationFiltration and evaporation
  9. customgave pale brown foam
  10. customthe insoluble solids were removed by filtration
  11. distillationthe solvent in the filtrate was distilled off under reduced pressure
  12. customThe solids thus obtained
  13. customwere purified by silica gel column chromatography (chloroform, methanol)

出典と根拠

ORDレコード
ord-95acb43618f342fbb4b5571b99e5bbf7
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08399464B2

反応ノート

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