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4,7-Dichloroquinoline → 3-Amino-5-[(7-chloroquinolin-4-yl)amino]benzonitrile hydrochloride

HRID 1190898
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인쇄 미리보기

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HRID 1190898 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([NH2:10])[CH:9]=1)[C:5]#[N:6].[Cl:11][C:12]1[C:21]2[C:16](=[CH:17][C:18]([Cl:22])=[CH:19][CH:20]=2)[N:15]=[CH:14][CH:13]=1>C(O)C>[ClH:11].[NH2:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([NH:10][C:12]2[C:21]3[C:16](=[CH:17][C:18]([Cl:22])=[CH:19][CH:20]=3)[N:15]=[CH:14][CH:13]=2)[CH:9]=1)[C:5]#[N:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 68664,7-DichloroquinolineHCID 128973293,5-Diaminobenzonitrile

생성물 1

HCID 672483483-Amino-5-[(7-chloroquinolin-4-yl)amino]benzonitrile hydrochloride수율 74.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

3,5-Diaminobenzonitrile (500 mg, 3.76 mmol) and 4,7-dichloroquinoline (744 mg, 1 eq) were stirred at room temperature in 50 mL of ethanol for 18 h. The precipitate was removed by filtration to yield expected compound as a yellow powder (925 mg, 74% yield).

후처리

  1. customThe precipitate was removed by filtration

출처 및 근거

ORD 기록
ord-e9d6932425db4a00a94ece4326dabe77
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08680095B2

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