반응식
[NH2:1][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]=1C(OCC)=O.Cl.[NH4+].[OH-]>>[C:7]1([N:6]2[C:2]([NH2:1])=[CH:3][CH:4]=[N:5]2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1참가 물질
4
실험 절차
5-Amino-4-carbethoxy-1-phenylpyrazole (1 eq.) was dissolved in 36% HCl solution (30 eq.) and the reaction mixture was stirred under reflux for overnight. The mixture was cooled, poured onto ice and made basic with NH4OH. The mixture was extracted with DCM (×3). The combined organic fractions were washed with brine, dried (Na2SO4), and the solvent was evaporated under reduced pressure to obtain the product as pale yellow oil in 94% yield. MS (ES+) C9H9N3 requires 159, found: 160 (M+H)+.
후처리
- temperatureunder reflux for overnight
- temperatureThe mixture was cooled
- additionpoured onto ice
- extractionThe mixture was extracted with DCM (×3)
- washThe combined organic fractions were washed with brine
- dry with materialdried (Na2SO4)
- customthe solvent was evaporated under reduced pressure
출처 및 근거
- ORD 기록
- ord-e2f183bfde9840139d413b9b940b96d3
- 출처 데이터셋
- uspto-grants-2013_06
- 특허 번호
- US08470823B2
연결된 노트
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