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Trifluoromethanesulfonic anhydride → HCID 57781104、化合物

HRID 1690713
ノート
印刷プレビュー

反応式

HRID 1690713 の反応式
FC(F)(F)S(OS(C(F)(F)F)(=O)=O)(=O)=O.C(N(C(C)C)CC)(C)C.[CH2:25]([N:27]([CH2:38][CH3:39])[C:28](=[O:37])[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=1[CH2:35]O)[CH3:26].C(OC([N:47]1[CH:51]=[C:50]([I:52])[N:49]=[CH:48]1)=O)(C)(C)C.C(=O)(O)[O-].[Na+]>ClCCl>[CH2:25]([N:27]([CH2:38][CH3:39])[C:28](=[O:37])[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=1[CH2:35][N:49]1[C:50]([I:52])=[CH:51][N:47]=[CH:48]1)[CH3:26]
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

7

反応物 5

HCID 67749Trifluoromethanesulfonic anhydrideHCID 81531DiisopropylethylamineHCID 516892Sodium BicarbonateHCID 13660025N,N-Diethyl-2-(hydroxymethyl)benzamideHCID 596566331-Boc-4-iodo-1H-imidazole

生成物 1

HCID 57781104HCID 57781104、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒3 回

反応条件

温度
-78 °C

実験手順

A flask is charged with dichloromethane (200 mL) and trifluoromethanesulfonic anhydride (19.34 g, 67.20 mmol) and cooled to −78° C. A solution of diisopropylethylamine (9.57 g, 73.30 mmol) and N,N-diethyl-2-hydroxymethyl-benzamide (12.92 g, 61.09 mmol) in dichloromethane (40 mL) is added over 10 min. After 30 min, a solution of 4-iodo-imidazole-1-carboxylic acid tert-butyl ester (12.83 g, 42.76 mmol) in dichloromethane (40 mL) is added. The mixture is allowed to gradually warm overnight and after 18 h, saturated aqueous sodium bicarbonate (100 mL) is added and the mixture is stirred vigorously for 30 min. The aqueous layer is extracted with dichloromethane. The combined organic phase is dried over MgSO4, filtered through a cotton plug and concentrated in vacuo. The residue is purified by silica gel flash chromatography (dichloromethane-methanol, 49:1) to afford N,N-diethyl-2-(5-iodo-imidazol-1-ylmethyl)-benzamide; MS (ESI) m/z 384.1 (M+H).

後処理

  1. waitThe mixture is allowed to gradually warm overnight and after 18 h
  2. extractionThe aqueous layer is extracted with dichloromethane
  3. dry with materialThe combined organic phase is dried over MgSO4
  4. filtrationfiltered through a cotton plug
  5. concentrationconcentrated in vacuo
  6. customThe residue is purified by silica gel flash chromatography (dichloromethane-methanol, 49:1)

出典と根拠

ORDレコード
ord-955b115f81f64e2180a5608b516dbc17
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08153674B2

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