Acrolein dimer → {(3,4-Dihydro-2H-pyran-2-yl)-[1-(2-dimethylamino-ethyl)-1H-tetrazol-5-yl]-methyl}-(3-imidazol-1-yl-propyl)-amine

HRID 18465

반응식

HRID 18465 반응식
[N:1]1([CH2:6][CH2:7][CH2:8][NH2:9])[CH:5]=[CH:4][N:3]=[CH:2]1.[O:10]1[CH:15]=[CH:14][CH2:13][CH2:12][CH:11]1[CH:16]=O.C[Si]([N:22]=[N+:23]=[N-:24])(C)C.[N+:25]([CH2:27][CH2:28][N:29]([CH3:31])[CH3:30])#[C-:26]>CO>[O:10]1[CH:15]=[CH:14][CH2:13][CH2:12][CH:11]1[CH:16]([NH:9][CH2:8][CH2:7][CH2:6][N:1]1[CH:5]=[CH:4][N:3]=[CH:2]1)[C:26]1[N:25]([CH2:27][CH2:28][N:29]([CH3:31])[CH3:30])[N:24]=[N:23][N:22]=1

참가 물질

6

반응물 4

HCID 60994Acrolein dimerHCID 78378AzidotrimethylsilaneHCID 787361H-Imidazole-1-propanamineHCID 27715502-Isocyano-N,N-dimethylethanamine

생성물 1

HCID 25059390{(3,4-Dihydro-2H-pyran-2-yl)-[1-(2-dimethylamino-ethyl)-1H-tetrazol-5-yl]-methyl}-(3-imidazol-1-yl-propyl)-amine

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

3-Imidazol-1-yl-propylamine (1 mmol) and 3,4-Dihydro-2H-pyran-2-carbaldehyde (1 mmol) were combined in methanol (2 ml, dry). After 2 hours Trimethylsilylazide (5 mmol) and (2-Isocyano-ethyl)-dimethyl-amine (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-859a5691f5d641a8b6aba2247b719733
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07741354B2

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