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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → HCID 60046937, 화합물

HRID 1672352
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HRID 1672352 반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([Cl:12])[CH:10]=2)[N:5]=[CH:4][C:3]=1[N+:13]([O-:15])=[O:14].[NH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.O>C(O)(=O)C>[Cl:12][C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][CH:8]=1)[N:5]=[CH:4][C:3]([N+:13]([O-:15])=[O:14])=[C:2]2[NH:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 6115AnilineHCID 106816704,6-Dichloro-3-nitroquinoline

생성물 1

HCID 60046937HCID 60046937, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

0.6 g (2.46 mmol) of 4,6-dichloro-3-nitro-quinoline (step c)) and 0.247 ml (2.71 mmol) of aniline in 4 ml of acetic acid are stirred at room temperature for 4 h (tlc-control). A precipitate is formed. The reaction mixture is poured into 150 ml of water. The solid is filtered off and washed with water and hexane. The filtrate is dissolved in ca. 50 ml of diethylether, filtered from insoluble material, and the solvent is evaporated. The residue (title compound, yellow crystals) is dried at 60° C. overnight. mp: 174-175° C.; ES-MS: m/e0=300.

후처리

  1. customA precipitate is formed
  2. filtrationThe solid is filtered off
  3. washwashed with water and hexane
  4. dissolutionThe filtrate is dissolved in ca. 50 ml of diethylether
  5. filtrationfiltered from insoluble material
  6. customthe solvent is evaporated
  7. dry with materialThe residue (title compound, yellow crystals) is dried at 60° C. overnight

출처 및 근거

ORD 기록
ord-52065cc8afe14fee9703b50145836a47
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07998972B2

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