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Iodine chloride → 1-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-5-(1-azido-2-iodoethyl)uracil

HRID 732925
ノート
印刷プレビュー

反応式

HRID 732925 の反応式
[I:1]Cl.[N-:3]=[N+:4]=[N-:5].[Na+].[OH:7][CH2:8][CH:9]([CH2:22][OH:23])[CH2:10][CH2:11][N:12]1[CH:19]=[C:18]([CH:20]=[CH2:21])[C:16](=[O:17])[NH:15][C:13]1=[O:14].C(Cl)(Cl)Cl.CO>C(#N)C>[OH:7][CH2:8][CH:9]([CH2:22][OH:23])[CH2:10][CH2:11][N:12]1[CH:19]=[C:18]([CH:20]([N:3]=[N+:4]=[N-:5])[CH2:21][I:1])[C:16](=[O:17])[NH:15][C:13]1=[O:14]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 24640Iodine chlorideHCID 33557Sodium AzideHCID 100372831-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-5-vinyluracilHCID 21584188Chloroform methanol

生成物 1

HCID 4903881-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-5-(1-azido-2-iodoethyl)uracil収率 21.3%

試薬・触媒・溶媒 1

HCID 6342
Acetonitrile
溶媒
2 回

反応条件

温度
0 °C

実験手順

Iodine monochloride (50 mg, 0.3 mmol) was added slowly with stirring during a five minute period to a suspension of sodium azide (72 mg, 1.1 mmol) in dry acetonitrile (10 ml) at ice-bath temperature with stirring. This mixture was stirred for a further 5 min., a solution of 20 (66 mg, 0.275 mmol) in dry acetonitrile (40 ml) was added, the reaction mixture was maintained at 0° C. for 30 min. with stirring. The resulting red-brown colored reaction mixture was poured onto ice cold water (25 ml), the mixture was extracted with ethyl acetate (3×50 ml) and the ethyl acetate extract was washed with 5% aqueous sodium thiosulfate (30 ml). Drying the colorless ethyl acetate fraction. (Na2SO4), removal of the solvent in vacuo and purification of the residue obtained by elution from a silica gel column using chloroform:methanol (90:10, v/v) as eluent afforded 21c (24 mg, 21%) as a viscous oil.

後処理

  1. stirringThis mixture was stirred for a further 5 min.
  2. stirringwith stirring
  3. additionThe resulting red-brown colored reaction mixture was poured onto ice cold water (25 ml)
  4. extractionthe mixture was extracted with ethyl acetate (3×50 ml)
  5. extractionthe ethyl acetate extract
  6. washwas washed with 5% aqueous sodium thiosulfate (30 ml)
  7. dry with materialDrying the colorless ethyl acetate fraction
  8. custom(Na2SO4), removal of the solvent
  9. customin vacuo and purification of the residue
  10. customobtained by elution from a silica gel column

出典と根拠

ORDレコード
ord-468575b97a7245ec9d3b434003cc29c2
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07589077B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート