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N-Methylisatoic anhydride → N-[3-(1H-Imidazol-1-yl)propyl]-2-(methylamino)benzamide

HRID 2164793
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인쇄 미리보기

반응식

HRID 2164793 반응식
C[N:2]1[C:8](=O)[O:7][C:5](=O)[C:4]2=[CH:10][CH:11]=[CH:12][CH:13]=[C:3]12.[N:14]1([CH2:19][CH2:20][CH2:21][NH2:22])[CH:18]=[CH:17][N:16]=[CH:15]1>O1CCOCC1>[CH3:8][NH:2][C:3]1[CH:13]=[CH:12][CH:11]=[CH:10][C:4]=1[C:5]([NH:22][CH2:21][CH2:20][CH2:19][N:14]1[CH:18]=[CH:17][N:16]=[CH:15]1)=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 25160N-Methylisatoic anhydrideHCID 787361H-Imidazole-1-propanamine

생성물 1

HCID 13280097N-[3-(1H-Imidazol-1-yl)propyl]-2-(methylamino)benzamide수율 69.8%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

N-Methylisatoic anhydride (17.7 g) was added in portions to a stirred solution of 3-imidazol-1-ylpropylamine (12.5 g) in dioxan (150 ml) over a period of 15 minutes. Stirring was continued for 40 minutes before the solution was evaporated in vacuo to give 2-methylamino-N-(3-imidazol-1-ylpropyl)benzamide (18.0 g), in the form of a buff coloured solid, m.p. 138°-141° C., after recrystallisation from isopropanol.

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후처리

  1. customwas evaporated in vacuo

출처 및 근거

ORD 기록
ord-908a83b5879847a88735022867ce69ea
출처 데이터셋
uspto-grants-1985_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04507315

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