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O-Xylene → 4-chloro-alpha,alpha-dimethyl-1H-imidazo[4,5-c]quinoline-1-ethanol

HRID 704851
노트
인쇄 미리보기

반응식

HRID 704851 반응식
[NH2:1][C:2]1[C:3]([Cl:18])=[N:4][C:5]2[C:10]([C:11]=1[NH:12][CH2:13][C:14]([CH3:17])([OH:16])[CH3:15])=[CH:9][CH:8]=[CH:7][CH:6]=2.[C:19]1(C)C(C)=CC=CC=1>C(OC(OCC)OCC)C>[Cl:18][C:3]1[C:2]2[N:1]=[CH:19][N:12]([CH2:13][C:14]([CH3:15])([CH3:17])[OH:16])[C:11]=2[C:10]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=2[N:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7237O-XyleneHCID 226726541-((3-Amino-2-chloroquinolin-4-yl)amino)-2-methylpropan-2-ol

생성물 1

HCID 98384584-chloro-alpha,alpha-dimethyl-1H-imidazo[4,5-c]quinoline-1-ethanol

시약·촉매·용매 1

HCID 31214Ethyl orthoformate용매

반응 조건

온도
80 °C

실험 절차

A suspension of 1-[(3-amino-2-chloro-4-quinolinyl)amino]-2-methyl-2-propanol (5 g from EXAMPLE 13) in xylene (50 mL) and triethylorthoformate (5 mL) was heated at 80° C. until no starting material remained as determined by thin layer chromatography. The resulting solution was cooled, and the precipitated product was isolated by filtration and washed with xylene (3×10 mL).

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후처리

  1. temperatureThe resulting solution was cooled
  2. customthe precipitated product was isolated by filtration
  3. washwashed with xylene (3×10 mL)

출처 및 근거

ORD 기록
ord-2f9de2be19964988a21def32afae6495
출처 데이터셋
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04988815

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