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

HRID 925293
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HRID 925293 반응식
[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
50 °C

실험 절차

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%).

후처리

  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)

출처 및 근거

ORD 기록
ord-3f1b4a33091b4491b39299e536c7653b
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09284296B2

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