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Trifluoroacetic acid → 2-(6-Morpholino-2,3-dioxoindolin-1-yl)acetic acid

HRID 571263
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반응식

HRID 571263 반응식
[O:1]1[CH2:6][CH2:5][N:4]([C:7]2[CH:15]=[C:14]3[C:10]([C:11](=[O:25])[C:12](=[O:24])[N:13]3[CH2:16][C:17]([O:19]C(C)(C)C)=[O:18])=[CH:9][CH:8]=2)[CH2:3][CH2:2]1.C(O)(C(F)(F)F)=O>C(Cl)Cl>[O:1]1[CH2:6][CH2:5][N:4]([C:7]2[CH:15]=[C:14]3[C:10]([C:11](=[O:25])[C:12](=[O:24])[N:13]3[CH2:16][C:17]([OH:19])=[O:18])=[CH:9][CH:8]=2)[CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 86681677Tert-butyl 2-(6-morpholino-2,3-dioxoindolin-1-yl)acetate

생성물 1

HCID 866816782-(6-Morpholino-2,3-dioxoindolin-1-yl)acetic acid수율 98.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of tert-butyl 2-(6-morpholino-2,3-dioxoindolin-1-yl)acetate (0.400 g, 1.155 mmol) in DCM (10 ml), TFA (1.716 ml, 23.10 mmol) was added drop wise. The resulting red solution was stirred at room temperature overnight. The volatiles were evaporated under vacuum to afford 2-(6-morpholino-2,3-dioxoindolin-1-yl)acetic acid (0.330 g, 1.137 mmol, 98% yield). MS/ESI+ 291.1 [MH]+.

후처리

  1. customThe volatiles were evaporated under vacuum

출처 및 근거

ORD 기록
ord-ef4fd2cb4f8a461c85f30b1a9ff85ee2
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09024027B2

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