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Ethyl imidazo[1,2-a]pyrazine-2-carboxylate → HCID 11845779, 화합물

HRID 2216552
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인쇄 미리보기

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HRID 2216552 반응식
[ClH:1].CCO.[CH2:5]([O:7][C:8]([C:10]1[N:11]=[C:12]2[CH:17]=[N:16][CH:15]=[CH:14][N:13]2[CH:18]=1)=[O:9])[CH3:6]>[Pd].CCO>[ClH:1].[CH2:5]([O:7][C:8]([C:10]1[N:11]=[C:12]2[CH2:17][NH:16][CH2:15][CH2:14][N:13]2[CH:18]=1)=[O:9])[CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 11845418Ethyl imidazo[1,2-a]pyrazine-2-carboxylateHCID 21887872Ethanol hydrochloride

생성물 1

HCID 11845779HCID 11845779, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

0.46 M HCl-EtOH (169 mL) and 10% Pd—C (50% wet) (1.37 g) were added to the EtOH (546 mL) solution of imidazo[1,2-a]pyrazine-2-carboxylic acid ethyl ester (13.7 g). The mixture was hydrogenated under H2 at 40 psi at room temperature for 15 h. The reaction mixture was filtered and Pd—C was washed with EtOH. The filtrate was concentrated under reduced pressure. The residue was applied to silica gel column chromatography, then the column was eluted with CHCl3-MeOH (9/1˜2/1). The titled compound was obtained as brown crystals Yield: 10.4 g, 63%.

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후처리

  1. filtrationThe reaction mixture was filtered
  2. washPd—C was washed with EtOH
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. washthe column was eluted with CHCl3-MeOH (9/1˜2/1)

출처 및 근거

ORD 기록
ord-8d77dd93ef5a4edcbf74a4742fb44cc8
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07112582B2

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