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5-Amino-2-isobutoxybenzonitrile → N-(3-Cyano-4-isobutoxyphenyl)-1,5-dimethylpyrazole-4-carboxamide

HRID 1744551
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인쇄 미리보기

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HRID 1744551 반응식
[CH3:1][N:2]1[C:6]([CH3:7])=[C:5]([C:8]([OH:10])=O)[CH:4]=[N:3]1.ON1C2C=CC=CC=2N=N1.[NH2:21][C:22]1[CH:23]=[CH:24][C:25]([O:30][CH2:31][CH:32]([CH3:34])[CH3:33])=[C:26]([CH:29]=1)[C:27]#[N:28]>C(O)C>[C:27]([C:26]1[CH:29]=[C:22]([NH:21][C:8]([C:5]2[CH:4]=[N:3][N:2]([CH3:1])[C:6]=2[CH3:7])=[O:10])[CH:23]=[CH:24][C:25]=1[O:30][CH2:31][CH:32]([CH3:33])[CH3:34])#[N:28]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 193660285-Amino-2-isobutoxybenzonitrileHCID 222282081-Hydroxybenzotriazole 1,5-dimethylpyrazole-4-carboxylate

생성물 1

HCID 22227889N-(3-Cyano-4-isobutoxyphenyl)-1,5-dimethylpyrazole-4-carboxamide수율 35.2%

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
78 °C

실험 절차

1-Hydroxybenzotriazole 1,5-dimethylpyrazole-4-carboxylate (2 g) and 5-amino-2-isobutoxybenzonitrile (1.9 g) were added to ethanol (25 ml) and the mixture was stirred at 78° C. for 3 h. After evaporation of the solvent, the residue was purified by silica gel column chromatography (mobile phase:chloroform:methanol=50:1) to give the title compound (0.8 g), melting point: 160–162° C.

후처리

  1. customAfter evaporation of the solvent
  2. customthe residue was purified by silica gel column chromatography (mobile phase:chloroform:methanol=50:1)

출처 및 근거

ORD 기록
ord-846c6aa5067241aa9992da7668f6cc3d
출처 데이터셋
uspto-grants-2006_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07015218B1

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