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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Azobisisobutyronitrile → HCID 86611703, 화합물

HRID 2390942
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인쇄 미리보기

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HRID 2390942 반응식
CC(N=NC(C#N)(C)C)(C#N)C.[Cl:13][C:14]1[N:19]=[C:18]2[S:20][N:21]=[C:22]([CH3:23])[C:17]2=[CH:16][CH:15]=1.[Br:24]NC(=O)CCC(N)=O>C(Cl)(Cl)(Cl)Cl>[Br:24][CH2:23][C:22]1[C:17]2[C:18](=[N:19][C:14]([Cl:13])=[CH:15][CH:16]=2)[S:20][N:21]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6547AzobisisobutyronitrileHCID 9834204N-BromosuccinamideHCID 146892486-Chloro-3-methyl[1,2]thiazolo[5,4-b]pyridine

생성물 1

HCID 86611703HCID 86611703, 화합물

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

반응 조건

온도
80 °C

실험 절차

AIBN (1.35 mmol) was added to a solution of 6-chloro-3-methylisothiazolo[5,4-b]pyridine (13.5 mmol) and N-bromosuccinamide (27.1 mmol) in carbon tetrachloride (25 mL). The reaction mixture was heated at 80° C. for 6 h, allowed to cool to rt, and the precipitated solids were removed by filtration. The filtrate was concentrated to provide crude 3-(bromomethyl)-6-chloroisothiazolo[5,4-b]pyridine as yellow oil.

후처리

  1. temperatureto cool to rt
  2. customthe precipitated solids were removed by filtration
  3. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-7be6d95886c14e828c3202c504564f44
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273891B2

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