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Ethyl bromopyruvate → 2-Amino-carbethoxycarbonylmethyl-quinoxalinium bromide

HRID 1632189
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HRID 1632189 반응식
[NH2:1][C:2]1[CH:11]=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[Br:12][CH2:13][C:14](=[O:20])[C:15]([O:17][CH2:18][CH3:19])=[O:16]>C(COC)OC>[Br-:12].[NH2:1][C:2]1[CH:11]=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N+:3]=1[CH2:13][C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 66144Ethyl bromopyruvateHCID 2245732-Aminoquinoxaline

생성물 1

HCID 202170592-Amino-carbethoxycarbonylmethyl-quinoxalinium bromide수율 74.9%

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

A solution of 0.9 g of 2-amino-quinoxaline, 1.25 g of ethyl bromopyruvate and 25 ml of dimethoxyethane was stirred overnight at room temperature and was filtered to obtain 1.58 g of 2-amino-carbethoxycarbonylmethyl-quinoxalinium bromide in the form of a pale yellow crystalline solid.

후처리

  1. filtrationwas filtered

출처 및 근거

ORD 기록
ord-4990518f5b4641cfb311a620fce80106
출처 데이터셋
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04474784

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