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Phenethyl isocyanate → 4-Oxo-3-phenethyl-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide

HRID 2098289
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HRID 2098289 반응식
[CH2:1]([N:9]=[C:10]=[O:11])[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[N+:12](=[C:14]1[N:18]=[CH:17][N:16]=[C:15]1[C:19]([NH2:21])=[O:20])=[N-:13]>CS(C)=O>[O:11]=[C:10]1[N:9]([CH2:1][CH2:2][C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=2)[N:13]=[N:12][C:14]2=[C:15]([C:19]([NH2:21])=[O:20])[N:16]=[CH:17][N:18]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 160602Phenethyl isocyanateHCID 534265854-Diazo-4H-imidazole-5-carboxamide

생성물 1

HCID 441285544-Oxo-3-phenethyl-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

Phenethyl isocyanate (0.441 g, 3 mmol) was added drop wise to a suspension of 5-diazoimidazole-4-carboxamide (0.274 g, 2 mmol) in dry dimethylsulfoxide (2.5 mL) at room temperature under nitrogen. The resulting mixture was stirred at room temperature overnight. The reaction was quenched by the addition of ice and the solid product (pale pink) was removed by filtration, washed with water and ethyl acetate, and recrystallised from chloroform to give the title compound. Yield: 0.259 g, 46%. IR vmax/cm−1 3132, 1743, 1668. 1H NMR δH (DMSO-d6) 3.14 (2H, t, J 7.4, CH2), 4.53 (2H, t, J 7.4, CH2), 7.21-7.33 (5H, m, ArH), 7.68 (1H, br s, NH), 7.81 (1H, br s, NH), 8.83 (1H, s, 6-H). δC 31.1, 34.6, 50.4, 127.1, 129.0, 129.2, 129.3, 131.2, 134.7, 138.2, 139.4, 162.0. MS Found 285.1161. Calc for (M+H): 285.1100. Found C, 55.0; H, 4.3; N, 29.4. Calc. for C13H12N6O3C 54.9; H 4.3; N, 29.6%.

후처리

  1. customThe reaction was quenched by the addition of ice
  2. customthe solid product (pale pink) was removed by filtration
  3. washwashed with water and ethyl acetate
  4. customrecrystallised from chloroform

출처 및 근거

ORD 기록
ord-260f8e5869e8456b98c9201fdb96c57a
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08450479B2

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