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Hydrazine hydrate (1:1) → 8-(3-Trifluoromethylphenyl)pyrido[2,3-d]pyridazin-5-(6H)-one

HRID 1653961
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인쇄 미리보기

반응식

HRID 1653961 반응식
[F:1][C:2]([F:21])([F:20])[C:3]1[CH:4]=[C:5]([CH:17]=[CH:18][CH:19]=1)[C:6]([C:8]1[N:16]=[CH:15][CH:14]=[CH:13][C:9]=1[C:10](O)=[O:11])=O.O.[NH2:23][NH2:24]>C(O)C>[F:1][C:2]([F:21])([F:20])[C:3]1[CH:4]=[C:5]([C:6]2[C:8]3[N:16]=[CH:15][CH:14]=[CH:13][C:9]=3[C:10](=[O:11])[NH:24][N:23]=2)[CH:17]=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 200788952-(3-Trifluoromethylbenzoyl)nicotinic acid

생성물 1

HCID 200788638-(3-Trifluoromethylphenyl)pyrido[2,3-d]pyridazin-5-(6H)-one

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 2-(3-trifluoromethylbenzoyl)nicotinic acid (1.5 g) and hydrazine hydrate (0.4 g) in ethanol was heated at the reflux temperature for 5 hours. On cooling and reduction of the volume of solvent by evaporation, a precipitate formed which was collected by filtration, to give the title compound as a white solid, 1.08 g, m.p. 210°-215° C.

후처리

  1. temperaturewas heated at the reflux temperature for 5 hours
  2. temperatureOn cooling
  3. customreduction of the volume of solvent by evaporation
  4. customa precipitate formed which
  5. filtrationwas collected by filtration

출처 및 근거

ORD 기록
ord-9fe5b2bec79f4dce9192e2e36735ee5b
출처 데이터셋
uspto-grants-1995_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05405826

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