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Hydrazine hydrate (1:1) → 3-(5-chlorothiophen-2-yl)-5-methyl-1H-pyrazole

HRID 2359066
ノート
印刷プレビュー

反応式

HRID 2359066 の反応式
[C:1]([C:4]1[S:5][C:6]([Cl:9])=[CH:7][CH:8]=1)(=O)[CH3:2].CO[C:12](OC)([N:14](C)C)[CH3:13].O.[NH2:20]N>CN(C)C(=O)C>[Cl:9][C:6]1[S:5][C:4]([C:1]2[CH:2]=[C:12]([CH3:13])[NH:14][N:20]=2)=[CH:8][CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 24654Hydrazine hydrate (1:1)HCID 805722-Acetyl-5-chlorothiopheneHCID 878351,1-Dimethoxyethyl(dimethyl)amine

生成物 1

HCID 52606203-(5-chlorothiophen-2-yl)-5-methyl-1H-pyrazole収率 71%

試薬・触媒・溶媒 1

HCID 31374Dimethylacetamide溶媒

反応条件

温度
90 °C

実験手順

A mixture of 2-acetyl-5-chlorothiophene (156 mmol) and N,N-dimethylacetamide dimethyl acetal (171 mmol) in 200 mL N,N-dimethylacetamide was heated to 90° C. for 4 h and then allowed to cool to room temperature. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in 200 mL absolute ethanol. Hydrazine monohydrate (234 mmol) was added and the mixture was stirred at room temperature for 24 h. The solvent was removed under vacuum. Petroleum ether was added and the precipitate formed was filtered then washed to afford 22 g (71% yield) 3-(5-chloro-2-thienyl)-5-methyl-1H-pyrazole.

後処理

  1. temperatureto cool to room temperature
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. dissolutionthe residue was dissolved in 200 mL absolute ethanol
  4. customThe solvent was removed under vacuum
  5. additionPetroleum ether was added
  6. customthe precipitate formed
  7. filtrationwas filtered
  8. washthen washed

出典と根拠

ORDレコード
ord-c96c5394755245c4929584072115aadf
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08685974B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート