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Methyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate → Methyl 10-methylacridan-9-carboxylate

HRID 68205
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인쇄 미리보기

반응식

HRID 68205 반응식
FC(F)(F)S([O-])(=O)=O.[CH3:9][N+:10]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[C:17]([C:24]([O:26][CH3:27])=[O:25])=[C:16]2[C:11]=1[CH:12]=[CH:13][CH:14]=[CH:15]2>CO>[CH3:9][N:10]1[C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:17]([C:24]([O:26][CH3:27])=[O:25])[C:16]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]1=2
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 86648905Methyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate

생성물 1

HCID 12813956Methyl 10-methylacridan-9-carboxylate

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of methyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate (75), 4.25 parts, in methanol is reduced as described in Example I to give 3.2 parts of methyl 10-methylacridan-9-carboxylate and the isolated product has the following structure confirmed by NMR.

출처 및 근거

ORD 기록
ord-e520dbfed13343b78f1b05d43e37b7af
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08822233B2

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