반응식
[C:1]([CH:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[C:5]#[N:6])(=O)[CH3:2].[NH:13]([CH:15](O)[CH3:16])[NH2:14].C[OH:19]>>[NH2:6][C:5]1[N:13]([CH2:15][CH2:16][OH:19])[N:14]=[C:1]([CH3:2])[C:4]=1[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1참가 물질
4
실험 절차
α-Acetylphenylacetonitrile (10 g) was dissolved in methanol (100 mL), and hydrazinoethanol (5.3 g) was added, and the mixture was heated under reflux for 4 hrs. After the completion of the reaction, the solvent was evaporated. The obtained residue was subjected to silica gel column chromatography, and the fraction eluted with chloroform:methanol=40:1 was concentrated to give 5-amino-1-(2-hydroxyethyl)-3-methyl-4-phenylpyrazole (11.4 g) as white crystals.
후처리
- temperaturethe mixture was heated
- temperatureunder reflux for 4 hrs
- customAfter the completion of the reaction
- customthe solvent was evaporated
- washthe fraction eluted with chloroform
- concentrationmethanol=40:1 was concentrated
출처 및 근거
- ORD 기록
- ord-60683cf36ac5418d8f27950efd500f7f
- 출처 데이터셋
- uspto-grants-2009_03
- 특허 번호
- US07501412B2
연결된 노트
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