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3-Aminocinnamic acid ethyl ester → Ethyl 3-[3-[[[6-(3-chlorophenyl)-2-pyridinyl]carbonyl]amino]phenyl]-2-propenoate

HRID 2053253
노트
인쇄 미리보기

반응식

HRID 2053253 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C:8]2[N:13]=[C:12]([C:14]([OH:16])=O)[CH:11]=[CH:10][CH:9]=2)[CH:5]=[CH:6][CH:7]=1.[CH2:17]([O:19][C:20](=[O:30])[CH:21]=[CH:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([NH2:29])[CH:24]=1)[CH3:18]>>[CH2:17]([O:19][C:20](=[O:30])[CH:21]=[CH:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([NH:29][C:14]([C:12]2[CH:11]=[CH:10][CH:9]=[C:8]([C:4]3[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[CH:3]=3)[N:13]=2)=[O:16])[CH:24]=1)[CH3:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 978253-Aminocinnamic acid ethyl esterHCID 247301356-(3-Chlorophenyl)picolinic acid

생성물 1

HCID 68497880Ethyl 3-[3-[[[6-(3-chlorophenyl)-2-pyridinyl]carbonyl]amino]phenyl]-2-propenoate

실험 절차

Carboxyilc acid (136)(44 mg, 0.19 mmol) was coupled with aniline (60)(40 mg, 0.21 mmol) using Method D. The residue was purified by column chromatography eluting with a stepped gradient of 10-15% EtOAc in heptane to give the title compound.

후처리

  1. customThe residue was purified by column chromatography
  2. washeluting with a stepped gradient of 10-15% EtOAc in heptane

출처 및 근거

ORD 기록
ord-0a2d7dfadd2a4205b88a54b4f522f121
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07326732B2

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