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Sodium Iodide → t-Butyl 2-(2-amino-4-thiazolyl)-2-[[(p-nitrobenzyloxycarbonyl)methoxy]imino]-acetate

HRID 1709370
ノート
印刷プレビュー

反応式

HRID 1709370 の反応式
[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:15]/[OH:16])/[C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[N:6]=1.Br[CH2:18][C:19]([O:21][CH2:22][C:23]1[CH:28]=[CH:27][C:26]([N+:29]([O-:31])=[O:30])=[CH:25][CH:24]=1)=[O:20].C(N(C(C)C)C(C)C)C.[I-].[Na+]>C(#N)C>[NH2:1][C:2]1[S:3][CH:4]=[C:5]([C:7](=[N:15][O:16][CH2:18][C:19]([O:21][CH2:22][C:23]2[CH:28]=[CH:27][C:26]([N+:29]([O-:31])=[O:30])=[CH:25][CH:24]=2)=[O:20])[C:8]([O:10][C:11]([CH3:13])([CH3:12])[CH3:14])=[O:9])[N:6]=1
参加物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 5238Sodium IodideHCID 81531DiisopropylethylamineHCID 70153214-Nitrobenzyl bromoacetateHCID 13826576tert-butyl 2-(2-amino-1,3-thiazol-4-yl)-2-(N-hydroxyimino)acetate

生成物 1

HCID 53971680t-Butyl 2-(2-amino-4-thiazolyl)-2-[[(p-nitrobenzyloxycarbonyl)methoxy]imino]-acetate収率 75.2%

試薬・触媒・溶媒 1

HCID 6342
Acetonitrile
溶媒

実験手順

6.1 g (25 mmol) of t-butyl 2-(2-amino-4-thiazolyl)-2-(Z)-hydroxyimino-acetate are dispersed in 250 ml of dry acetonitrile. 13.7 g (50 mmol) of p-nitrobenzyl bromoacetate and 12.9 ml (75 mmol) of N-ethyldiisopropylamine are now added thereto at room temperature while stirring. 7.5 g (50 mmol) of sodium iodide are added thereto 5 minutes later. The mixture is stirred at room temperature for 3.5 hours in an argon atmosphere. The solvent is subsequently removed by evaporation and the residue is diluted with 500 ml of ethyl acetate. The solution obtained is washed four times with a total of 2 l of water. The aqueous phase is extracted with 300 ml of ethyl acetate and the combined ethyl acetate solutions are dried over sodium sulphate and evaporated to dryness. After crystallization from ethyl acetate/hexane, there are obtained 8.2 g (75%) of t-butyl 2-(2-amino-4-thiazolyl)-2-[[(p-nitrobenzyloxycarbonyl)methoxy]imino]-acetate of melting point 146.8° C. (decomposition).

後処理

  1. custom5 minutes
  2. stirringThe mixture is stirred at room temperature for 3.5 hours in an argon atmosphere
  3. customThe solvent is subsequently removed by evaporation
  4. additionthe residue is diluted with 500 ml of ethyl acetate
  5. customThe solution obtained
  6. washis washed four times with a total of 2 l of water
  7. extractionThe aqueous phase is extracted with 300 ml of ethyl acetate
  8. dry with materialthe combined ethyl acetate solutions are dried over sodium sulphate
  9. customevaporated to dryness
  10. customAfter crystallization from ethyl acetate/hexane, there

出典と根拠

ORDレコード
ord-ad64373f7cac4d498097ffb671b1544e
出典データセット
uspto-grants-1990_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04948898

反応ノート

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