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Hydrochloric Acid → 6-Methylpyridine-3-sulfonyl chloride

HRID 1012517
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HRID 1012517 반응식
[CH3:1][C:2]1[N:7]=[CH:6][C:5](N)=[CH:4][CH:3]=1.[ClH:9].N([O-])=O.[Na+].[S:14]([O-:17])(O)=[O:15].[Na+]>O.S([O-])([O-])(=O)=O.[Cu+2]>[CH3:1][C:2]1[N:7]=[CH:6][C:5]([S:14]([Cl:9])(=[O:17])=[O:15])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric Acid2회HCID 2433135-Amino-2-methylpyridineHCID 23665763Sodium BisulfiteHCID 23668193Sodium Nitrite

생성물 1

HCID 223987146-Methylpyridine-3-sulfonyl chloride수율 15%

시약·촉매·용매 2

HCID 24462Copper Sulfate
촉매
HCID 962Water용매2회

실험 절차

To a mixture of 6-methylpyridine-3-amine (449 mg) and concentrated hydrochloric acid (5 mL) was added a solution of sodium nitrite (857 mg) in water (2 mL) at 0° C., and the mixture was stirred at the same temperature for 10 min. To the mixture was added a solution of concentrated hydrochloric acid (2.5 mL), copper sulfate (69 mg) and sodium hydrogen sulfite (5.08 g) in water (8 mL) at 0° C., and the mixture was stirred at room temperature for 30 min. The reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate=10:1) to give the title compound as a pale-yellow solid (yield 0.12 g, 15%).

후처리

  1. stirringthe mixture was stirred at room temperature for 30 min
  2. extractionThe reaction mixture was extracted with ethyl acetate
  3. washThe extract was washed with saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate=10:1)

출처 및 근거

ORD 기록
ord-f0b66a6e841c4bbea4494f66ff0b766e
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07977488B2

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