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Sodium Hydroxide → 2-Ethylthiazolo[4,5-c]quinoline

HRID 1199979
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반응식

HRID 1199979 반응식
[NH2:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([C:11]=1[SH:12])=[CH:9][CH:8]=[CH:7][CH:6]=2.[C:13](OC(=O)CC)(=O)[CH2:14][CH3:15].[OH-].[Na+]>Cl>[CH2:14]([C:15]1[S:12][C:11]2[C:10]3[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=3[N:4]=[CH:3][C:2]=2[N:1]=1)[CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 31263Propionic anhydrideHCID 1785079903-Aminoquinoline-4-thiol

생성물 1

HCID 150279042-Ethylthiazolo[4,5-c]quinoline수율 90%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

A mixture of 17.62 g (0.1 mole) of 3-amino-4-mercapto-quinoline and 85 ml of propionic anhydride is first slowly heated to boiling and then refluxed for one hour and a half. The reaction mixture is added dropwise to 800 ml of 1% aqueous hydrochloric acid under vigorous stirring. The homogenous solution is made alkaline to pH 10 by adding sodium hydroxide solution and extracted three times with 200 ml of benzene each. The benzene solution is evaporated. Thus 19.26 g of 2-ethylthiazolo[4,5-c]quinoline are obtained, yield 90%, m.p.: 48°-49° C.

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후처리

  1. temperatureis first slowly heated
  2. temperaturerefluxed for one hour
  3. extractionextracted three times with 200 ml of benzene each
  4. customThe benzene solution is evaporated

출처 및 근거

ORD 기록
ord-23e264946d404672b45bc35b0d549f8a
출처 데이터셋
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04904669

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