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Ethyl 3-methylthiazolo(3,2-a)benzimidazole-2-carboxylate → HCID 18003012, 화합물

HRID 478845
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인쇄 미리보기

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HRID 478845 반응식
C([O:3][C:4]([C:6]1[S:17][C:9]2=[N:10][C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[N:8]2[C:7]=1[CH3:18])=O)C.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[OH:3][CH2:4][C:6]1[S:17][C:9]2=[N:10][C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[N:8]2[C:7]=1[CH3:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12289498Ethyl 3-methylthiazolo(3,2-a)benzimidazole-2-carboxylateHCID 21226445Aluminium lithium hydride

생성물 1

HCID 18003012HCID 18003012, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Under ice-cooling, 3-methylthiazolo[3,2-a]benzoimidazole-2-carboxylic acid ethyl ester (Can. J. Chem., 45 (23), 2903-2912 (1967) (10 g) was added to THF (250 ml) suspension of LiAlH4 (1.46 g) and stirred at the same temperature for 1 hour. While cooling, the reaction solution was mixed with Na2SO4.10H2O and stirred, and then the insoluble matter was removed by filtration and the solvent was evaporated under a reduced pressure to obtain the title compound (6.36 g).

후처리

  1. temperatureUnder ice-cooling
  2. temperatureWhile cooling
  3. stirringstirred
  4. customthe insoluble matter was removed by filtration
  5. customthe solvent was evaporated under a reduced pressure

출처 및 근거

ORD 기록
ord-6152f59b288f485191185f9dc089a1be
출처 데이터셋
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06642264B1

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