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2-Chloroacetophenone → 3Chloro-2-methyl-7-phenacylpyrrolo-[2,3-b]pyridinehydrochloride

HRID 1756050
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인쇄 미리보기

반응식

HRID 1756050 반응식
[Cl:1][C:2]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[NH:4][C:3]=1[CH3:11].Cl[CH2:13][C:14]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:15]>CC#N>[ClH:1].[Cl:1][C:2]1[C:10]2[C:5]([N:6]([CH2:13][C:14]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[O:15])[CH:7]=[CH:8][CH:9]=2)=[N:4][C:3]=1[CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 107572-ChloroacetophenoneHCID 193925933-Chloro-2-methyl-1H-pyrrolo[2,3-b]pyridine

생성물 1

HCID 193926053Chloro-2-methyl-7-phenacylpyrrolo-[2,3-b]pyridinehydrochloride수율 134.9%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A solution of 200 mg (1.2 mmol) of 3-chloro-2-methyl pyrrolo-[2,3-b]pyridine and 204 mg (1,3 mmol) of 2-chloroacetophenon in 10 ml of CH3CN was refluxed for 48 h. The reaction mixture was cooled to room temperature and stirred for one hour. The precipitate was filtered off to give 260 mg (67%) of 3chloro-2-methyl-7-phenacylpyrrolo-[2,3-b]pyridinehydrochloride.

후처리

  1. filtrationThe precipitate was filtered off

출처 및 근거

ORD 기록
ord-e4bc02c4e71b48c0b008201024215e37
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05439917

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