1-Methylimidazole → (S)-N-[1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl]-4-oxo-4-phenylbutanamide

HRID 424881

反応式

HRID 424881 の反応式
[C:1]([CH2:9][CH2:10][C:11]([OH:13])=O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN1C=CN=C1.C1(C)C=CC(S(Cl)(=O)=O)=CC=1.[CH2:31]([C:33]1[N:34]=[C:35]([C@@H:38]([NH2:49])[CH2:39][C:40]2[CH:45]=[CH:44][C:43]([N+:46]([O-:48])=[O:47])=[CH:42][CH:41]=2)[S:36][CH:37]=1)[CH3:32]>C(Cl)Cl>[CH2:31]([C:33]1[N:34]=[C:35]([C@@H:38]([NH:49][C:11](=[O:13])[CH2:10][CH2:9][C:1](=[O:8])[C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH2:39][C:40]2[CH:45]=[CH:44][C:43]([N+:46]([O-:48])=[O:47])=[CH:42][CH:41]=2)[S:36][CH:37]=1)[CH3:32]

参加物

6

実験手順

3-Benzoylpropionic acid (0.250 g) is dissolved in CH2Cl2 (5 mL), N-methyl imidazole (0.333 mL) is added and the resulting solution is cooled to 0° C. after which a solution of p-toluenesulfonyl chloride (0.320 g) in CH2Cl2 (2 mL) is added dropwise. After 0.5 hours (S)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethanamine, 3, (0.388 g) is added. The reaction is stirred for 18 hours at room temperature and then concentrated in vacuo. The resulting residue is dissolved in EtOAc and washed with 1N HCl and brine. The solution is dried over Na2SO4, filtered, and concentrated and the crude material purified over silica to afford 0.415 g of the desired product.

後処理

  1. additionis added dropwise
  2. concentrationconcentrated in vacuo
  3. dissolutionThe resulting residue is dissolved in EtOAc
  4. washwashed with 1N HCl and brine
  5. dry with materialThe solution is dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customthe crude material purified over silica

出典と根拠

ORDレコード
ord-6b0e7d0dd83147b2a4c466ddbd9eada2
出典データセット
uspto-grants-2012_01
特許番号
US08106078B2

関連ノート

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