Azidotrimethylsilane → 2-[[1-(2,2-Dimethyl-propyl)-1H-tetrazol-5-yl]-(3-imidazol-1-yl-propylamino)-methyl]-quinolin-8-ol

HRID 18467

반응식

HRID 18467 반응식
[N:1]1([CH2:6][CH2:7][CH2:8][NH2:9])[CH:5]=[CH:4][N:3]=[CH:2]1.[OH:10][C:11]1[CH:12]=[CH:13][CH:14]=[C:15]2[C:20]=1[N:19]=[C:18]([CH:21]=O)[CH:17]=[CH:16]2.C[Si]([N:27]=[N+:28]=[N-:29])(C)C.[N+:30]([CH2:32][C:33]([CH3:36])([CH3:35])[CH3:34])#[C-:31]>CO>[CH3:34][C:33]([CH3:36])([CH3:35])[CH2:32][N:30]1[C:31]([CH:21]([NH:9][CH2:8][CH2:7][CH2:6][N:1]2[CH:5]=[CH:4][N:3]=[CH:2]2)[C:18]2[CH:17]=[CH:16][C:15]3[C:20](=[C:11]([OH:10])[CH:12]=[CH:13][CH:14]=3)[N:19]=2)=[N:29][N:28]=[N:27]1

참가 물질

6

실험 절차

3-Imidazol-1-yl-propylamine (1 mmol) and 8-Hydroxy-quinoline-2-carbaldehyde (1 mmol) were combined in methanol (2 ml, dry). After 2 hours Trimethylsilylazide (5 mmol) and 1-Isocyano-2,2-dimethyl-propane (1 mmol) was added. The reaction was stirred at room temperature for 48 h. After evaporation of the solvent the residue was purified with chromatographic methods.

후처리

  1. customAfter evaporation of the solvent the residue
  2. customwas purified with chromatographic methods

출처 및 근거

ORD 기록
ord-3470187e804f4bbabac598a8116168a6
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07741354B2

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