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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3,4,6-Trichloropyridazine → 3,6-Dichloro-4-methanesulfonylpyridazine

HRID 1524520
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HRID 1524520 반응식
[Cl:1][C:2]1[N:3]=[N:4][C:5]([Cl:9])=[CH:6][C:7]=1Cl.[Na+].[CH3:11][S:12]([O-:14])=[O:13]>O.C1COCC1.CN(C=O)C>[Cl:1][C:2]1[N:3]=[N:4][C:5]([Cl:9])=[CH:6][C:7]=1[S:12]([CH3:11])(=[O:14])=[O:13]
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참가 물질

4

반응물 2

HCID 951233,4,6-TrichloropyridazineHCID 2733271Sodium methanesulfinate

생성물 1

HCID 580457893,6-Dichloro-4-methanesulfonylpyridazine

시약·촉매·용매 1

HCID 86606902water THF DMF용매

실험 절차

3,4,6-Trichloropyridazine (2.5 g; 13.6 mmol) and methanesulfinic acid sodium salt (2.78 g, 27.26 mmol) were stirred in 20 ml of a solvent mixture of water/THF/DMF (5:10:5) at RT for 30 h. The solvent was removed under reduced pressure and the residue was partitioned between ethyl acetate and saturated ammonium chloride solution. The organic phase was removed and concentrated, and the crude product was purified by flash chromatography (dichloromethane:methanol). Yield: 1.4 g

후처리

  1. customThe solvent was removed under reduced pressure
  2. customthe residue was partitioned between ethyl acetate and saturated ammonium chloride solution
  3. customThe organic phase was removed
  4. concentrationconcentrated
  5. customthe crude product was purified by flash chromatography (dichloromethane:methanol)

출처 및 근거

ORD 기록
ord-2a4c6fcd11624d588d842a8da755c32f
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09079906B2

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