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Chlorosuccinimide → 6-Acetyl-8-chloropyrrolo[1,2-a]pyrazine

HRID 233461
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HRID 233461 반응식
[C:1]([C:4]1[N:8]2[CH:9]=[CH:10][N:11]=[CH:12][C:7]2=[CH:6][CH:5]=1)(=[O:3])[CH3:2].[Cl:13]N1C(=O)CCC1=O>C(Cl)(Cl)Cl>[C:1]([C:4]1[N:8]2[CH:9]=[CH:10][N:11]=[CH:12][C:7]2=[C:6]([Cl:13])[CH:5]=1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31398ChlorosuccinimideHCID 233564476-Acetylpyrrolo[1,2-a]pyrazine

생성물 1

HCID 233565286-Acetyl-8-chloropyrrolo[1,2-a]pyrazine수율 82.3%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

0.5 g of 6-acetylpyrrolo[1,2-a]pyrazine prepared in Preparation Example 15 was dissolved in 5 ml of chloroform; and 0.5 g of N-chlorosuccinimide was added threrto. The reaction mixture was refluxed for 2 hours and then concentrated. The residue was chromatographed over silica gel to yield 0.5 g of title compound.

후처리

  1. temperatureThe reaction mixture was refluxed for 2 hours
  2. concentrationconcentrated
  3. customThe residue was chromatographed over silica gel

출처 및 근거

ORD 기록
ord-1edb7d926dc94e7492f482ea5d86756f
출처 데이터셋
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05593984

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