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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ammonia → 2-Chloro-4-methylpyridine-3-carboxamide

HRID 2396584
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HRID 2396584 반응식
[Cl:1][C:2]1[C:7]([C:8](O)=[O:9])=[C:6]([CH3:11])[CH:5]=[CH:4][N:3]=1.O=S(Cl)Cl.[NH3:16]>C1(C)C=CC=CC=1>[Cl:1][C:2]1[C:7]([C:8]([NH2:16])=[O:9])=[C:6]([CH3:11])[CH:5]=[CH:4][N:3]=1
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참가 물질

5

반응물 3

HCID 222AmmoniaHCID 24386Thionyl ChlorideHCID 154837662-Chloro-4-methylpyridine-3-carboxylic acid

생성물 1

HCID 109428862-Chloro-4-methylpyridine-3-carboxamide수율 91%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a mixture of 2-chloro-4-methyl-3-pyridinecarboxylic acid (24.7 g, 157 mmol) and 75 mL of toluene at 70° C. was added 75 mL of SOCl2 (22.6 g, 190 mmol) within a period of 1 hour. The reaction mixture was refluxed for 4 hours and the resulting solution was cooled to room temperature. Dry NH3 gas was introduced at such a rate so as to maintain the internal temperature below 30° C. After removing toluene, the solid residue was washed successively with cold water and methanol, and dried to yield 22.72 g of the title compound (91%, m.p. 168°-170° C.).

후처리

  1. temperatureThe reaction mixture was refluxed for 4 hours
  2. temperatureto maintain the internal temperature below 30° C
  3. customAfter removing toluene
  4. washthe solid residue was washed successively with cold water and methanol
  5. customdried

출처 및 근거

ORD 기록
ord-7153c737860b4ca2803911bb6ce5a8eb
출처 데이터셋
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05493028

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