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Ethyl 3-oxopyrrolidine-1-carboxylate → 1-Ethoxycarbonyl-3-{5-fluoro-3-[4-(2-methyl1,3-dioxolan-2-yl)phenylthio]phenyl}-3-hydroxypyrrolidine

HRID 37562
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HRID 37562 반응식
[F:1][C:2]1[CH:3]=[C:4]([S:9][C:10]2[CH:15]=[CH:14][C:13]([C:16]3([CH3:21])[O:20][CH2:19][CH2:18][O:17]3)=[CH:12][CH:11]=2)[CH:5]=[C:6](Br)[CH:7]=1.[CH2:22]([O:24][C:25]([N:27]1[CH2:31][CH2:30][C:29](=[O:32])[CH2:28]1)=[O:26])[CH3:23]>>[CH2:22]([O:24][C:25]([N:27]1[CH2:31][CH2:30][C:29]([C:6]2[CH:7]=[C:2]([F:1])[CH:3]=[C:4]([S:9][C:10]3[CH:15]=[CH:14][C:13]([C:16]4([CH3:21])[O:20][CH2:19][CH2:18][O:17]4)=[CH:12][CH:11]=3)[CH:5]=2)([OH:32])[CH2:28]1)=[O:26])[CH3:23]
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참가 물질

3

반응물 2

HCID 277754Ethyl 3-oxopyrrolidine-1-carboxylateHCID 199358785-Fluoro-3-[4-(2-methyl-1,3-dioxolan-2-yl)phenylthio]bromobenzene

생성물 1

HCID 199358391-Ethoxycarbonyl-3-{5-fluoro-3-[4-(2-methyl1,3-dioxolan-2-yl)phenylthio]phenyl}-3-hydroxypyrrolidine수율 50%

실험 절차

Using an analogous procedure to that described in the fourth paragraph of the portion of Example 28 which is concerned with the preparation of starting materials, 5-fluoro-3-[4-(2-methyl-1,3-dioxolan-2-yl)phenylthio]bromobenzene was reacted with 1-ethoxycarbonylpyrrolidin-3-one to give 1-ethoxycarbonyl-3-{5-fluoro-3-[4-(2-methyl1,3-dioxolan-2-yl)phenylthio]phenyl}-3-hydroxypyrrolidine as a gum in 50% yield.

출처 및 근거

ORD 기록
ord-8b71f0028fff4b4bb96b8fcd4a9c2f1d
출처 데이터셋
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05420298

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