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Ethyl chloroformate → Methyl 2-[(ethoxycarbonyl)amino]-5-ethylthiophene-3-carboxylate

HRID 1889298
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인쇄 미리보기

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HRID 1889298 반응식
[NH2:1][C:2]1[S:3][C:4]([CH2:11][CH3:12])=[CH:5][C:6]=1[C:7]([O:9][CH3:10])=[O:8].Cl[C:14]([O:16][CH2:17][CH3:18])=[O:15]>C1(C)C=CC=CC=1>[CH2:17]([O:16][C:14]([NH:1][C:2]1[S:3][C:4]([CH2:11][CH3:12])=[CH:5][C:6]=1[C:7]([O:9][CH3:10])=[O:8])=[O:15])[CH3:18]
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참가 물질

4

반응물 2

HCID 10928Ethyl chloroformateHCID 7370942-Amino-5-ethyl-3-thiophenecarboxylic acid methyl ester

생성물 1

HCID 59351565Methyl 2-[(ethoxycarbonyl)amino]-5-ethylthiophene-3-carboxylate수율 92%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
100 °C

실험 절차

A mixture of methyl 2-amino-5-ethylthiophene-3-carboxylate (7.07 g), ethyl chloroformate (4.4 mL) and toluene (100 mL) was stirred at 100° C. for 3 hr. The reaction mixture was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography to give the title compound as colorless oil (9 g, 92%).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customthe obtained residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-f6cad9811457482fb2f981cfae7d4920
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501750B2

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