Hydrazine → Oxadiazole

HRID 1746142

反応式

HRID 1746142 の反応式
COC(=O)[C:4]1[CH:9]=[C:8]([OH:10])[CH:7]=[C:6](F)[CH:5]=1.Br[C:14]1[CH:18]=[CH:17][O:16][N:15]=1.[NH2:19][NH2:20].C([C:23](CC)(CC)[C:24]([O-:27])([O-])[O-])C>CO.O.C(OCC)(=O)C>[O:10]([C:14]1[CH2:18][CH2:17][O:16][N:15]=1)[C:8]1[CH:9]=[CH:4][CH:5]=[CH:6][CH:7]=1.[O:27]1[CH:24]=[CH:23][N:20]=[N:19]1

参加物

9

実験手順

3-(phenoxy)-4,5-dihydroisoxazole I-224a and I-224b were prepared in 3 steps according to the following procedures: 3-fluoro-5-hydroxybenzoic acid methyl ester is reacted with racemic bromoisoxazole I-14 using Method 5. The resulting methyl ester (1.0 equiv) is dissolved in methanol (0.08 M) after which hydrazine (50 equiv, 50% by weight in water) is added and the reaction is allowed to stir for 14 h. The reaction mixture is then concentrated under vacuum and used directly in the next step. Triethylorthoacetate (8.0 equiv) is added and the reaction is sealed and heated to reflux for 14 h. The reaction is then transferred to a separatory funnel with excess ethyl acetate and water. The organic layer was washed water and brine, drive over sodium sulfate and concentrated under vacuum to provide crude material which was purified using flash silica gel chromatography (gradient ethyl acetate/hexanes) to provide the desired racemic oxadiazole I-224. These compounds can be separated using chiral HPLC methods known in the art. For example, see chiral HPLC Method disclosed herein. [M+H]+=424.5 m/z. Activity: A

後処理

  1. additionis added
  2. concentrationThe reaction mixture is then concentrated under vacuum
  3. customthe reaction is sealed
  4. temperatureheated
  5. temperatureto reflux for 14 h
  6. washThe organic layer was washed water and brine, drive over sodium sulfate
  7. concentrationconcentrated under vacuum
  8. customto provide crude material which
  9. customwas purified

出典と根拠

ORDレコード
ord-f7273679920a4fa4902cc15ea65bfa4c
出典データセット
uspto-grants-2015_10
特許番号
US09149465B2

関連ノート

読み込み中…