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Hydrogen Peroxide → HCID 59474741, 화합물

HRID 1966555
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HRID 1966555 반응식
[OH:1]O.[Cl:3][C:4]1[CH:5]=[C:6]([CH:22]=[CH:23][C:24]=1[Cl:25])[CH2:7][NH:8][C:9]1[C:18]2[C:13](=[C:14]([S:19][CH3:20])[CH:15]=[CH:16][CH:17]=2)[N:12]=[C:11]([CH3:21])[CH:10]=1>C(O)(=O)C>[Cl:3][C:4]1[CH:5]=[C:6]([CH:22]=[CH:23][C:24]=1[Cl:25])[CH2:7][NH:8][C:9]1[C:18]2[C:13](=[C:14]([S:19]([CH3:20])=[O:1])[CH:15]=[CH:16][CH:17]=2)[N:12]=[C:11]([CH3:21])[CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 784Hydrogen PeroxideHCID 59474731HCID 59474731, 화합물

생성물 1

HCID 59474741HCID 59474741, 화합물수율 35.5%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

H2O2 (30%, 20.0 mg, 0.55 mmole) was added dropwise to a solution of (3,4-dichlorobenzyl)-(2-methyl-8-methylsulfanylquinolin-4-yl)-amine (100 mg, 0.275 mmole) in acetic acid (3.5 mL) at 0° C. The mixture was stirred at RT for 16 hrs, concentrated by half, 2N NaOH was added and the resulting mixture was extracted with ethyl acetate. The organic phases were dried and concentrated. Precipitation in isopropyl ether gave the product as a white solid (37 mg, 35%).

후처리

  1. concentrationconcentrated by half, 2N NaOH
  2. additionwas added
  3. extractionthe resulting mixture was extracted with ethyl acetate
  4. customThe organic phases were dried
  5. concentrationconcentrated
  6. customPrecipitation in isopropyl ether

출처 및 근거

ORD 기록
ord-16248eb833664be7ab8f09f82bca8827
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08420670B2

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