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Hydrogen Peroxide → HCID 59474756, 화합물

HRID 1966556
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인쇄 미리보기

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HRID 1966556 반응식
[OH:1]O.[Cl:3][C:4]1[CH:5]=[C:6]([CH:23]=[CH:24][C:25]=1[Cl:26])[CH2:7][NH:8][C:9]1[C:18]2[C:13](=[C:14]([S:19]([CH3:21])=[O:20])[CH:15]=[CH:16][CH:17]=2)[N:12]=[C:11]([CH3:22])[CH:10]=1>C(O)(=O)C>[Cl:3][C:4]1[CH:5]=[C:6]([CH:23]=[CH:24][C:25]=1[Cl:26])[CH2:7][NH:8][C:9]1[C:18]2[C:13](=[C:14]([S:19]([CH3:21])(=[O:1])=[O:20])[CH:15]=[CH:16][CH:17]=2)[N:12]=[C:11]([CH3:22])[CH:10]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 784Hydrogen PeroxideHCID 59474741HCID 59474741, 화합물

생성물 1

HCID 59474756HCID 59474756, 화합물수율 61.3%

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
70 °C

실험 절차

H2O2 (30%, 18.0 mg, 0.53 mmole) was added dropwise to a solution of (3,4-dichlorobenzyl)-(8-methanesulfinyl-2-methylquinolin-4-yl)-amine (50 mg, 0.132 mmole) in acetic acid (3.5 mL) at 0° C. The mixture was stirred at 70° C. 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 ethyl acetate gave the product as white solid (32 mg, 61%).

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 ethyl acetate

출처 및 근거

ORD 기록
ord-2c0e5f55bb8c4ec58b7ef2a507473288
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08420670B2

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