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2-Amino-carbethoxycarbonylmethyl-quinoxalinium bromide → Ethyl imidazo[1,2-a]quinoxaline-2-carboxylate

HRID 1632190
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반응식

HRID 1632190 반응식
[Br-].[NH2:2][C:3]1[CH:12]=[N:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N+:4]=1[CH2:13][C:14]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=O>C(O)C>[CH:13]1[N:4]2[C:5]3[C:10]([N:11]=[CH:12][C:3]2=[N:2][C:14]=1[C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:9][CH:8]=[CH:7][CH:6]=3
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 202170592-Amino-carbethoxycarbonylmethyl-quinoxalinium bromide

생성물 1

HCID 13228325Ethyl imidazo[1,2-a]quinoxaline-2-carboxylate수율 88.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A suspension of 0.4 g of the product of Step A in 15 ml of ethanol was refluxed for 2 hours and the resulting clear orange solution was concentrated to half its volume. The mixture was filtered to obtain 0.25 g of ethyl imidazo-[1,2-a]-quinoxaline-2-carboxylate as a pale yellow solid which were crystallized from an ether-methanol mixture to obtain the product in the form of soft-white needles melting at 184°-187° C. with decomposition.

후처리

  1. temperaturewas refluxed for 2 hours
  2. concentrationthe resulting clear orange solution was concentrated to half its volume
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • filtrationThe mixture was filtered
  • 출처 및 근거

    ORD 기록
    ord-3eed3d6c2027478faec535b2ba90feb1
    출처 데이터셋
    uspto-grants-1984_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04474784

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