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Ethyl chloroformate → 1-(4-Ethoxycarbonylaminophenyl)pyrrole

HRID 1167463
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반응식

HRID 1167463 반응식
Cl[C:2]([O:4][CH2:5][CH3:6])=[O:3].[NH2:7][C:8]1[CH:13]=[CH:12][C:11]([N:14]2[CH:18]=[CH:17][CH:16]=[CH:15]2)=[CH:10][CH:9]=1>N1C=CC=CC=1>[CH2:5]([O:4][C:2]([NH:7][C:8]1[CH:9]=[CH:10][C:11]([N:14]2[CH:18]=[CH:17][CH:16]=[CH:15]2)=[CH:12][CH:13]=1)=[O:3])[CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10928Ethyl chloroformateHCID 27954574-Pyrrol-1-yl-phenylamine

생성물 1

HCID 149198291-(4-Ethoxycarbonylaminophenyl)pyrrole

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

Ethyl chloroforrnate (0.38 ml) was added dropwisc to a stirred solution of 1-(4-aminophenyl)pyrrole (0.56 g, 3.54 mmol , Corelli et al., Farmaco. Ed. Sci., 1983, 38, 219) in pyridine (5 ml) at 5-10° C. for 15 minutes. The cooling bath was removed and stirring continued for 1.5 hours. The mixture was evaporated and the residue was purified by flash column chromatography on silica gel, eluting with a gradient of 1-4% MeOH in dichloromethane to give the title product (0.43 g) as a solid.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. customThe cooling bath was removed
  2. customThe mixture was evaporated
  3. customthe residue was purified by flash column chromatography on silica gel
  4. washeluting with a gradient of 1-4% MeOH in dichloromethane

출처 및 근거

ORD 기록
ord-1ed62850dab7449f904cee0391797b40
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06617339B1

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