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Pyridine → Ethyl 2-[3-fluoro-4-(metylsulfonylamino)phenyl]propionate

HRID 238922
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인쇄 미리보기

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HRID 238922 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH3:12])[C:9]([O-:11])=[O:10])=[CH:4][C:3]=1[F:13].[CH3:14][S:15](Cl)(=[O:17])=[O:16].N1C=CC=[CH:21][CH:20]=1>>[F:13][C:3]1[CH:4]=[C:5]([CH:8]([CH3:12])[C:9]([O:11][CH2:20][CH3:21])=[O:10])[CH:6]=[CH:7][C:2]=1[NH:1][S:15]([CH3:14])(=[O:17])=[O:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 1049PyridineHCID 31297Methanesulfonyl chlorideHCID 866091712-(4-Amino-3-fluorophenyl)propionate

생성물 1

HCID 24754385Ethyl 2-[3-fluoro-4-(metylsulfonylamino)phenyl]propionate수율 91%

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온도
0 °C

실험 절차

A solution of 2-(4-amino-3-fluorophenyl)propionate (1-13, 4 mM) and pyridine (10 ml) was dissoluted with methansulfonylchloride (6 mM) and was stirred at 0° C. for 10 minutes. The combined organic layers were washed with H2O and residue was purified by flash column chromatography on silica gel with EtOAc/hexanes (1:2) as eluant to afford ethyl 2-[3-fluoro-4-(metylsulfonylamino)phenyl]propionate compound (1-26, SU-658).

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. washThe combined organic layers were washed with H2O and residue
  2. customwas purified by flash column chromatography on silica gel with EtOAc/hexanes (1:2) as eluant

출처 및 근거

ORD 기록
ord-116ba5f3ec5347fcaaf9cd8bda8012b5
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08642657B2

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