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Methyl iodide → 1-Isopropyl-2-methylsulfanyl-1H-imidazole-4,5-dione

HRID 2212104
ノート
印刷プレビュー

反応式

HRID 2212104 の反応式
[CH:1]([NH:4][C:5]([NH2:7])=[S:6])([CH3:3])[CH3:2].IC.[CH2:10](N(CC)CC)C.[C:17](Cl)(=[O:21])[C:18](Cl)=[O:19]>CC(C)=O.C(Cl)Cl>[CH:1]([N:4]1[C:18](=[O:19])[C:17](=[O:21])[N:7]=[C:5]1[S:6][CH3:10])([CH3:3])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 6328Methyl iodideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 1711921Urea, 1-isopropyl-2-thio-

生成物 1

HCID 116655211-Isopropyl-2-methylsulfanyl-1H-imidazole-4,5-dione

試薬・触媒・溶媒 2

HCID 180Acetone溶媒
HCID 6344
Dichloromethane
溶媒

実験手順

Isopropyl thiourea 9 (8.0 g, 67.7 mmol) in 100 ml of dry acetone was added iodomethane (6.3 ml, 101 mmol) dropwise at room temperature. After the addition was completed, the mixture was refluxed for 1 hour, and the solvent was evaporated to dryness under the reduced pressure to give a gum. The gummy hydroiodide salt was suspended in 200 ml of dry methylene chloride and to the suspension was added triethylamine (37.7 ml, 270 mmol). The mixture was stirred for 30 minutes at room temperature, cooled down to −78° C. with a dry ice/acetone bath. To the mixture was added dropwise oxalyl chloride (40.6 ml of 2M solution, 81.2 mmol) and stirred at −78° C. for 1 hour. The reaction was quenched by addition of water to decompose the excess oxalyl chloride, the solvent was dried over Na2SO4 and evaporated to dryness in vacuo.

後処理

  1. additionAfter the addition
  2. temperaturethe mixture was refluxed for 1 hour
  3. customthe solvent was evaporated to dryness under the reduced pressure
  4. customto give a gum
  5. temperaturecooled down to −78° C. with a dry ice/acetone bath
  6. stirringstirred at −78° C. for 1 hour
  7. customThe reaction was quenched by addition of water
  8. dry with materialthe solvent was dried over Na2SO4
  9. customevaporated to dryness in vacuo

出典と根拠

ORDレコード
ord-7225e4e670a849dc983aa77980caefcf
出典データセット
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07101902B2

反応ノート

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