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Sulfuric Acid → 5-Amino-1-(o-tolyl)-1H-pyrazole-4-carboxamide

HRID 1666211
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HRID 1666211 반응식
S(=O)(=O)(O)O.[NH2:6][C:7]1[N:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])[N:10]=[CH:9][C:8]=1[C:19]#[N:20].[OH-:21].[Na+]>>[NH2:6][C:7]1[N:11]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])[N:10]=[CH:9][C:8]=1[C:19]([NH2:20])=[O:21]
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참가 물질

4

반응물 3

HCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 121505575-amino-1-(2-methylphenyl)-1H-pyrazole-4-carbonitrile

생성물 1

HCID 119839075-Amino-1-(o-tolyl)-1H-pyrazole-4-carboxamide

반응 조건

온도
40 °C

실험 절차

300 ml of 96% strength sulphuric acid are cautiously added to 40.0 g (201.8 mmol) of 5-amino-1-(2-methylphenyl)-1H-pyrazole-4-carbonitrile (Example 8A) while cooling in ice. The mixture is then heated to 40° C. and stirred for 2 hours at this temperature. After cooling, it is poured into 2 l of ice-water and cautiously neutralized with 50% strength sodium hydroxide solution. After extraction with ethyl acetate three times (2 l each time) the combined organic phases are washed with saturated sodium chloride solution and dried over sodium sulphate, and the solvent is distilled off under reduced pressure. 36.0 g (82% of theory) of product (purity >90%) are obtained and are employed without further purification in subsequent reactions.

후처리

  1. temperaturewhile cooling in ice
  2. temperatureAfter cooling
  3. extractionAfter extraction with ethyl acetate three times (2 l each time) the combined organic phases
  4. washare washed with saturated sodium chloride solution
  5. dry with materialdried over sodium sulphate
  6. distillationthe solvent is distilled off under reduced pressure
  7. custom36.0 g (82% of theory) of product (purity >90%) are obtained
  8. customare employed without further purification in subsequent reactions

출처 및 근거

ORD 기록
ord-304be8fe34f54ed7823d160a0c6087c5
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08044060B2

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