Aminoacetaldehyde dimethyl acetal → 1-(3-bromophenyl)-1,3-dihydro-2H-imidazol-2-one

HRID 471829

反応式

HRID 471829 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([N:8]=[C:9]=[O:10])[CH:3]=1.CO[CH:13](OC)[CH2:14][NH2:15]>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([N:8]2[CH:13]=[CH:14][NH:15][C:9]2=[O:10])[CH:5]=[CH:6][CH:7]=1

参加物

4

実験手順

A solution of 1-bromo-3-isocyanatobenzene (1.0 mL, 8.01 mmol) and [2,2-bis(methyloxy)ethyl]amine (0.86 mL, 8.01 mmol) in CH2Cl2 (15 mL) was stirred at room temperature for 16 hr. The solution was concentrated in vacuo and the residue taken up in a mixture of CH3CN (10 mL) and H2O (3 mL). TFA (3 mL) was added and the solution stirred at room temperature for 4 hr. The solution was concentrated in vacuo, the residue taken up in EtOAc then washed with satd NaHCO3, H2O, and brine. The organics were then dried over Na2SO4, concentrated in vacuo and the residue recrystallized from EtOAc to give 1-(3-bromophenyl)-1,3-dihydro-2H-imidazol-2-one as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 6.60 (d, J=3.0 Hz, 1H), 7.03 (d, J=3.0 Hz, 1H), 7.34-7.36 (m, 2H); 7.70-7.72 (m, 1H), 8.06 (s, 1H), 10.39 (br s, 1H).

後処理

  1. concentrationThe solution was concentrated in vacuo
  2. additionthe residue taken up in a mixture of CH3CN (10 mL) and H2O (3 mL)
  3. additionTFA (3 mL) was added
  4. concentrationThe solution was concentrated in vacuo
  5. washthen washed with satd NaHCO3, H2O, and brine
  6. dry with materialThe organics were then dried over Na2SO4
  7. concentrationconcentrated in vacuo
  8. customthe residue recrystallized from EtOAc

出典と根拠

ORDレコード
ord-52dbd0b5fbc84d94965fd20a4fe80c67
出典データセット
uspto-grants-2014_01
特許番号
US08633175B2

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