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Aluminium lithium hydride → [3-Amino-5-(1-methyl-1H-tetrazol-5-yl)-phenyl]-methanol

HRID 241695
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인쇄 미리보기

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HRID 241695 반응식
C([O:3][C:4](=O)[C:5]1[CH:10]=[C:9]([C:11]2[N:15]([CH3:16])[N:14]=[N:13][N:12]=2)[CH:8]=[C:7]([NH2:17])[CH:6]=1)C.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[NH2:17][C:7]1[CH:6]=[C:5]([CH2:4][OH:3])[CH:10]=[C:9]([C:11]2[N:15]([CH3:16])[N:14]=[N:13][N:12]=2)[CH:8]=1
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참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 667334833-Amino-5-(1-methyl-1H-tetrazol-5-yl)-benzoic acid ethyl ester

생성물 1

HCID 22252683[3-Amino-5-(1-methyl-1H-tetrazol-5-yl)-phenyl]-methanol수율 33.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of 3-Amino-5-(1-methyl-1H-tetrazol-5-yl)-benzoic acid ethyl ester (250 mg) in THF (5 ml) at 0° C. was added pre-cooled 1M LiAlH4 solution in THF (2 ml) dropwise. This was stirred for 3 h. The reaction mixture was poured onto ice-water and extracted into EtOAc. The organic layer was separated, dried and concentrated in vacuum. Flash chromatography (100:0 to 95:5 gradient DCM:MeOH) afforded the title compound (70 mg).

후처리

  1. additionThe reaction mixture was poured onto ice-water
  2. extractionextracted into EtOAc
  3. customThe organic layer was separated
  4. customdried
  5. concentrationconcentrated in vacuum

출처 및 근거

ORD 기록
ord-249b192e6c5a4decb183b4c10bf73440
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08653075B2

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