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Ethylamine → 5-bromo-1-phenyl-N-ethyl-1H-pyrazole-4-carboxamide

HRID 1731265
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반응식

HRID 1731265 반응식
[Br:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:5]=[CH:4][C:3]=1[C:13]([OH:15])=O.C(N1C=CN=C1)([N:18]1[CH:22]=[CH:21]N=C1)=O.C(N)C>CN(C=O)C>[Br:1][C:2]1[N:6]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:5]=[CH:4][C:3]=1[C:13]([NH:18][CH2:22][CH3:21])=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6341EthylamineHCID 682631,1'-CarbonyldiimidazoleHCID 138219315-bromo-1-phenyl-1H-pyrazole-4-carboxylic acid

생성물 1

HCID 138219365-bromo-1-phenyl-N-ethyl-1H-pyrazole-4-carboxamide수율 34.9%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of 2.6 g of 5-bromo-1-phenyl-1H-pyrazole-4-carboxylic acid and 2.4 g of carbonyldiimidazole in 50 ml DMF was stirred at room temperature for 30 minutes. Five milliliters of 70% aqueous ethylamine was next added to the solution and the mixture was stirred for an additional two hours at room temperature. The reaction mixture was poured into ice water and the precipitated solid was collected by filtration. The solid was recrystallized from ethanol to afford 1.0 g of 5-bromo-1-phenyl-N-ethyl-1H-pyrazole-4-carboxamide. Yield 34%. mp=158°-160° C.

후처리

  1. filtrationthe precipitated solid was collected by filtration
  2. customThe solid was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-29283ee7967e47b6ba6d7e8ac1caa042
출처 데이터셋
uspto-grants-1986_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04620865

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