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1-Nitro-9-phenoxyacridine → HCID 12391509, 화합물

HRID 1390533
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HRID 1390533 반응식
[N+:1]([C:4]1[C:17]2[C:8](=[N:9][C:10]3[C:15]([C:16]=2OC2C=CC=CC=2)=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH:7]=[CH:6][CH:5]=1)([O-:3])=[O:2].[ClH:25].Cl.[CH2:27]([NH:31][CH2:32][CH2:33][NH2:34])[CH:28]([CH3:30])[CH3:29]>C1(O)C=CC=CC=1>[ClH:25].[ClH:25].[N+:1]([C:4]1[C:17]2[C:8](=[N:9][C:10]3[C:15]([C:16]=2[NH:34][CH2:33][CH2:32][NH:31][CH2:27][CH:28]([CH3:30])[CH3:29])=[CH:14][CH:13]=[CH:12][CH:11]=3)[CH:7]=[CH:6][CH:5]=1)([O-:3])=[O:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 131933931-Nitro-9-phenoxyacridineHCID 21332743HCID 21332743, 화합물

생성물 1

HCID 12391509HCID 12391509, 화합물

시약·촉매·용매 1

HCID 996Phenol용매

반응 조건

온도
90 °C

실험 절차

1-Nitro-9-phenoxyacridine (1.58 g) is dissolved in about 5 g of phenol, and then 0.95 g of 2-isobutylaminoethylamine dihydrochloride is added and is heated at a temperature of 90° C. for 1.2 hour. It is isolated in a similar manner, as in Example VII. There is obtained 1-nitro-9-isobutylaminoethylaminoacridine dihydrochloride with a melting point of 230° C. (with decomposition).

후처리

  1. customIt is isolated in a similar manner, as in Example VII

출처 및 근거

ORD 기록
ord-5b679c64b23c4fb283e4da3038897f60
출처 데이터셋
uspto-grants-1979_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04139531

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