Hydrochloric Acid → 1-(5-Chloro-2-methoxyphenyl)-5-phenyl-2,4-imidazolidinedione

HRID 362457

反応式

HRID 362457 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:12][CH3:13])=[C:6]([NH:8][C:9]([NH2:11])=[O:10])[CH:7]=1.O.[C:15]1([C:21]([CH:23]=[O:24])=O)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.Cl.[K+].[Br-]>C(O)C.C(O)(=O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:12][CH3:13])=[C:6]([N:8]2[CH:21]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[C:23](=[O:24])[NH:11][C:9]2=[O:10])[CH:7]=1

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 253877Potassium BromideHCID 347398(5-Chloro-2-methoxyphenyl)ureaHCID 12215922Glyoxal, phenyl-, hydrate

生成物 1

HCID 158387761-(5-Chloro-2-methoxyphenyl)-5-phenyl-2,4-imidazolidinedione

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 702Ethanol溶媒

実験手順

N-(5-Chloro-2-methoxyphenyl)urea (1 g, 5 mmol) and phenylglyoxal monohydrate (760 mg, 5 mmol) were taken up in absolute ethanol (100 ml) and acetic acid (1 ml) and 1 ml of conc. HCl added. The reaction mixture was heated at reflux 3.5 h and allowed to stand at 24° C. for 18 h prior to concentration by rotary evaporation. The residue was dissolved in ethyl acetate, washed with sat'd NaHCO3 solution and brine. Recrystallization from methylene chloride/hexanes gave 1 g (63%) mp 200° C.; IR(KBr, ν=cm-1) 3168, 3064, 1772, 1701, 1504, 1444, 1426, 1408, 1260, 1190, 1150; 1H NMR (300 MHz, CDCl3) δ3.59 (3H, s), 5.60 (1H, s), 6.80 (1H, d, J=8.8 Hz), 7.14-7.37 (7H, m), 8.92 (1H, br.s); MS(DCl)m/z: 317(MH+)

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux 3.5 h
  3. concentrationto concentration
  4. customby rotary evaporation
  5. dissolutionThe residue was dissolved in ethyl acetate
  6. washwashed with sat'd NaHCO3 solution and brine
  7. customRecrystallization from methylene chloride/hexanes
  8. customgave 1 g (63%) mp 200° C.

出典と根拠

ORDレコード
ord-e519e9c2037a47c4a1d8a7fc4bd135b7
出典データセット
uspto-grants-1999_02
特許番号
US05869509

関連ノート

読み込み中…