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Salicylaldehyde → 3-Salicylideneamino-1-(2-pyridyl)-2-pyrazoline

HRID 1589666
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HRID 1589666 반응식
[NH2:1][C:2]1[CH2:6][CH2:5][N:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)[N:3]=1.[CH:13](=O)[C:14]1[C:15](=[CH:17][CH:18]=[CH:19][CH:20]=1)[OH:16]>CO>[CH:13](=[N:1][C:2]1[CH2:6][CH2:5][N:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)[N:3]=1)[C:14]1[C:15](=[CH:17][CH:18]=[CH:19][CH:20]=1)[OH:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6998SalicylaldehydeHCID 134966252-(3-Amino-2-pyrazolin-1-yl)pyridine

생성물 1

HCID 1361510013-Salicylideneamino-1-(2-pyridyl)-2-pyrazoline

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

3-Amino-1-(2-pyridyl)-2-pyrazoline (1.6 g) and salicylaldehyde (1.2 g) were dissolved together with methanol (16 ml). The resulting solution was heated to reflux and after about 15 minutes a crystalline solid separated. After another 15 minutes at reflux the suspension was cooled and the separated 3-salicylideneamino-1-(2-pyridyl)-2-pyrazoline was re-crystallized from methanol m.p. 242°-243° (yield 500 mg).

후처리

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  • temperatureThe resulting solution was heated
  • temperatureto reflux and after about 15 minutes a crystalline solid
  • customseparated
  • temperatureAfter another 15 minutes at reflux the suspension
  • temperaturewas cooled
  • customthe separated 3-salicylideneamino-1-(2-pyridyl)-2-pyrazoline was re-crystallized from methanol m.p. 242°-243° (yield 500 mg)
  • 출처 및 근거

    ORD 기록
    ord-c6bf792821cb4f62a37ed934ad504742
    출처 데이터셋
    uspto-grants-1986_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04572913

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