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Hydrazine hydrate (1:1) → HCID 19592850, 화합물

HRID 613546
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HRID 613546 반응식
Cl[C:2]1[C:11]2[C:6](=[C:7]([NH:12][C:13](=[O:22])[C:14]3[C:19]([Cl:20])=[CH:18][CH:17]=[CH:16][C:15]=3[Cl:21])[CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][CH:3]=1.O.[NH2:24][NH2:25]>C(O)C.CN1CCCC1=O>[Cl:21][C:15]1[CH:16]=[CH:17][CH:18]=[C:19]([Cl:20])[C:14]=1[C:13]([NH:12][C:7]1[CH:8]=[CH:9][CH:10]=[C:11]2[C:6]=1[N:5]=[CH:4][CH:3]=[C:2]2[NH:24][NH2:25])=[O:22]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 195925644-Chloro-8-(2,6-dichlorobenzoylamino)quinoline

생성물 1

HCID 19592850HCID 19592850, 화합물수율 87.6%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 13387N-methyl-2-pyrrolidone용매

반응 조건

온도
100 °C

실험 절차

A mixture of 4-chloro-8-(2,6-dichlorobenzoylamino)quinoline (200 mg) and hydrazine monohydrate (285 mg) in ethanol (4 ml) and N-methylpyrrolidone (1 ml) was heated at 100° C. overnight. After cooling, the resulting precipitates were collected by filtration, and the residue was recrystallized from ethanol to give 8-(2,6-dichlorobenzoylamino)-4-hydrazinoquinoline (173 mg).

후처리

  1. temperatureAfter cooling
  2. customthe resulting precipitates
  3. filtrationwere collected by filtration
  4. customthe residue was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-83ac8aead5504492aafd71d3ce9ff309
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06008230

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