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Acetaldehyde → 3-(Acridin-9-yl)amino-5-(ethylideneamino)phenylmethanol

HRID 1167992
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인쇄 미리보기

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HRID 1167992 반응식
[CH:1]1[C:14]2[C:5](=[N:6][C:7]3[C:12]([C:13]=2[NH:15][C:16]2[CH:17]=[C:18]([CH:20]=[C:21]([CH2:23][OH:24])[CH:22]=2)[NH2:19])=[CH:11][CH:10]=[CH:9][CH:8]=3)[CH:4]=[CH:3][CH:2]=1.[CH:25](=O)[CH3:26]>ClCCl.N1C=CC=CC=1>[CH:1]1[C:14]2[C:5](=[N:6][C:7]3[C:12]([C:13]=2[NH:15][C:16]2[CH:22]=[C:21]([CH2:23][OH:24])[CH:20]=[C:18]([N:19]=[CH:25][CH3:26])[CH:17]=2)=[CH:11][CH:10]=[CH:9][CH:8]=3)[CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 177AcetaldehydeHCID 3804823-(9-Acridinylamino)-5-hydroxymethylaniline

생성물 1

HCID 229948353-(Acridin-9-yl)amino-5-(ethylideneamino)phenylmethanol수율 80.1%

시약·촉매·용매 1

HCID 21875418Pyridine methylene chloride용매

실험 절차

3-(9-acridinylamino)-5-(hydroxymethyl)aniline was dissolved in dichloromethane/pyridine(1/1, v/v, 40 ml), and thereto acetaldehyde (2.09 g, 47.56 mmol) was added. The resulting mixture was stirred for 5 hours, and the solvent used was removed under the reduced pressure. Then, the resulting product was purified by column chromatography to give the titled compound.

후처리

  1. customthe solvent used was removed under the reduced pressure
  2. customThen, the resulting product was purified by column chromatography

출처 및 근거

ORD 기록
ord-8721ff2cffa6455aa9491308a5beb31e
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06620936B2

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