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4-Nitro-2,2'-bipyridine-N-oxide → 4-Methylsulfanyl-[2,2']bipyridinyl 1-oxide

HRID 925293
ノート
印刷プレビュー

反応式

HRID 925293 の反応式
[CH3:1][S-:2].[Na+].[N+]([C:7]1[CH:8]=[C:9]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=2)[N+:10]([O-:13])=[CH:11][CH:12]=1)([O-])=O>CN(C)C=O>[CH3:1][S:2][C:7]1[CH:8]=[C:9]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=2)[N+:10]([O-:13])=[CH:11][CH:12]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 33312824-Nitro-2,2'-bipyridine-N-oxideHCID 4378561Sodium methanethiolate

生成物 1

HCID 592012924-Methylsulfanyl-[2,2']bipyridinyl 1-oxide収率 22%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
50 °C

実験手順

Sodium thiomethoxide (1.06 g, 15.2 mmol) was added at 25° C. to 4-Nitro-[2,2′]bipyridinyl 1-oxide (3.0 g, 13.8 mmol) in dimethyl formamide (15 mL) and stirred for 2 hours at 50° C. The reaction mixture was added into ice (200 g) under vigorous stirring, the solid formed was filtered and washed with water (100 mL) and ether (100 mL), the filtrate was concentrated, diluted with water, extracted with dichloromethane (3×100 mL), dried with anhydrous sodium sulphate, filtered and concentrated under reduced pressure. The crude was purified by column chromatography on silica gel (0-100% Ethyl acetate in Hexane) to afford 4-methylsulfanyl-[2,2′]bipyridinyl 1-oxide as a white solid (650.0 mg, 22%).

後処理

  1. customthe solid formed
  2. filtrationwas filtered
  3. washwashed with water (100 mL) and ether (100 mL)
  4. concentrationthe filtrate was concentrated
  5. additiondiluted with water
  6. extractionextracted with dichloromethane (3×100 mL)
  7. dry with materialdried with anhydrous sodium sulphate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe crude was purified by column chromatography on silica gel (0-100% Ethyl acetate in Hexane)

出典と根拠

ORDレコード
ord-3f1b4a33091b4491b39299e536c7653b
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09284296B2

反応ノート

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