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Hydrochloric Acid → 1-(4-Methoxyphenyl)-1H-pyrazol-3-amine

HRID 394806
ノート
印刷プレビュー

反応式

HRID 394806 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH:13]=[CH:12][C:11]([NH:14]C(OC)=O)=[N:10]2)=[CH:5][CH:4]=1.[OH-].[K+].Cl>O.CO.C(OCC)(=O)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([N:9]2[CH:13]=[CH:12][C:11]([NH2:14])=[N:10]2)=[CH:7][CH:8]=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

6

反応物 3

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 543443991-[(4-Methoxy)phenyl]-3-[(methoxycarbonyl)amino]-1H-pyrazole

生成物 1

HCID 167406551-(4-Methoxyphenyl)-1H-pyrazol-3-amine収率 94.4%

試薬・触媒・溶媒 2

HCID 8857Ethyl Acetate溶媒HCID 22242641
Methanol--water (1/1)
溶媒

反応条件

温度
70 °C

実験手順

To a solution of 1-[(4-methoxy)phenyl]-3-[(methoxycarbonyl)amino]-1H-pyrazole-5-[(2′-aminosulfonyl-[1,1′]-biphen-4-yl)carboxyamide (0.22 g, 0.42 mmol) in 10 mL of 1:1 water/methanol was added potassium hydroxide (2.0 g, 35 mmol). The resulting mixture was stirred at 70° C. for 4 h and then was cooled to ambient temperature and was acidified with aq HCl. The reaction mixture was diluted with ethyl acetate and the organics were washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by prep HPLC (C18 reverse phase column, elution with a H2O/CH3CN gradient with 0.5% TFA) and lyophilized to afford 75 mg (38%) of the title compound as a white powder. LRMS (ES+): 463.8 (M+H)+.

後処理

  1. temperaturewas cooled to ambient temperature
  2. washthe organics were washed with brine
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by prep HPLC (
  6. washC18 reverse phase column, elution with a H2O/CH3CN gradient with 0.5% TFA) and

出典と根拠

ORDレコード
ord-0fd9d9d60cae4a5fbca71f5eecb75d4a
出典データセット
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06602895B2

反応ノート

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