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Hydrochloric Acid → 6-Chloro-2-methylpyridine-3-sulfonyl chloride

HRID 2070450
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HRID 2070450 반응식
[ClH:1].N[C:3]1[CH:4]=[CH:5][C:6]([Cl:10])=[N:7][C:8]=1[CH3:9].N([O-])=O.[Na+].[S:15](=[O:17])=[O:16]>O>[Cl:10][C:6]1[N:7]=[C:8]([CH3:9])[C:3]([S:15]([Cl:1])(=[O:17])=[O:16])=[CH:4][CH:5]=1
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 1119Sulfur DioxideHCID 70095003-Amino-6-chloro-2-picolineHCID 23668193Sodium Nitrite

생성물 1

HCID 552070736-Chloro-2-methylpyridine-3-sulfonyl chloride수율 67%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Under ice-cooling, thionyl chloride (4 mL) was added dropwise to water (24 mL) over 20 min. The mixture was stirred at room temperature for 12 hr to give a sulfur dioxide-containing solution. Separately, to the concentrated hydrochloric acid (6 mL) was added 5-amino-2-chloro-6-methylpyridine (1.0 g) with stirring under ice-cooling, and a solution of sodium nitrite (0.5 g) in water (2 mL) was added dropwise over 10 min. The reaction mixture was gradually added at 5° C. to the above-mentioned sulfur dioxide-containing solution added with cuprous chloride (10 mg). Under ice-cooling, the mixture was further stirred for 30 min, and the precipitate was collected by filtration, and washed with water to give the title compound as a pale-yellow solid (yield 1.1 g, 67%).

후처리

  1. additioncontaining solution
  2. temperaturecooling
  3. additioncontaining solution
  4. temperatureUnder ice-cooling
  5. stirringthe mixture was further stirred for 30 min
  6. filtrationthe precipitate was collected by filtration
  7. washwashed with water

출처 및 근거

ORD 기록
ord-9ea0bccd0fee430ba13093e8d173c208
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08299261B2

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