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Benzoyl Peroxide → 3-(Bromomethyl)isothiazolo[5,4-b]pyridine

HRID 424642
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반응식

HRID 424642 반응식
[Br:1]NC(=O)CCC(N)=O.[CH3:10][C:11]1[C:19]2[C:14](=[N:15][CH:16]=[CH:17][CH:18]=2)[S:13][N:12]=1.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[Br:1][CH2:10][C:11]1[C:19]2[C:14](=[N:15][CH:16]=[CH:17][CH:18]=2)[S:13][N:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7187Benzoyl PeroxideHCID 9834204N-BromosuccinamideHCID 124969753-Methyl-[1,2]thiazolo[5,4-b]pyridine

생성물 1

HCID 667026993-(Bromomethyl)isothiazolo[5,4-b]pyridine

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

N-Bromosuccinamide (10.7 mmol) was added to a solution of 3-methylisothiazolo[5,4-b]pyridine (10.0 mmol) in carbontetrachloride (20 mL). Benzoyl peroxide (0.82 mmol) was added and the reaction mixture was heated at reflux for 48 h. The reaction mixture was filtered through Celite (ethyl acetate) and the eluent was concentrated to provide crude 3-(bromomethyl)isothiazolo[5,4-b]pyridine as a yellow solid.

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureat reflux for 48 h
  3. filtrationThe reaction mixture was filtered through Celite (ethyl acetate)
  4. concentrationthe eluent was concentrated

출처 및 근거

ORD 기록
ord-b478c96bbd39448c9af2860e121b0708
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08106066B2

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