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1-Aminopyrrolidin-2-one → 5-cyclopentyl-N-(2-oxopyrrolidin-1-yl)-6-(2,2,2-trifluoroethoxy)-3-pyridinecarboxamide

HRID 240705
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인쇄 미리보기

반응식

HRID 240705 반응식
[CH:1]1([C:6]2[CH:7]=[C:8]([C:18]([OH:20])=O)[CH:9]=[N:10][C:11]=2[O:12][CH2:13][C:14]([F:17])([F:16])[F:15])[CH2:5][CH2:4][CH2:3][CH2:2]1.[NH2:21][N:22]1[CH2:26][CH2:25][CH2:24][C:23]1=[O:27]>>[CH:1]1([C:6]2[CH:7]=[C:8]([C:18]([NH:21][N:22]3[CH2:26][CH2:25][CH2:24][C:23]3=[O:27])=[O:20])[CH:9]=[N:10][C:11]=2[O:12][CH2:13][C:14]([F:15])([F:16])[F:17])[CH2:2][CH2:3][CH2:4][CH2:5]1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 124949741-Aminopyrrolidin-2-oneHCID 712941865-Cyclopentyl-6-(2,2,2-trifluoroethoxy)-3-pyridinecarboxylic acid

생성물 1

HCID 712943175-cyclopentyl-N-(2-oxopyrrolidin-1-yl)-6-(2,2,2-trifluoroethoxy)-3-pyridinecarboxamide

실험 절차

The title compound was synthesized in analogy to Example 1 using 5-cyclopentyl-6-(2,2,2-trifluoro-ethoxy)-3-pyridinecarboxylic acid (example 14c) and 1-amino-2-pyrrolidinone (CAN 6837-14-5) as starting materials; MS (EI) 372.1 (M+H)+.

출처 및 근거

ORD 기록
ord-c3354e4d30fe43639c214b081e3cc6b4
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
이 페이지에서참가 물질실험 절차출처 및 근거반응 노트
특허 번호
US08648099B2

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