Pyridine → N-[1-(2-Benzyloxy-ethyl)-2-oxo-propyl]-4-bromo-2-fluoro-benzamide

HRID 1445762ノート

反応式

HRID 1445762 の反応式
[C:1](OC(=O)C)(=O)C.N1C=CC=CC=1.[CH2:14]([O:21][CH2:22][CH2:23][CH:24]([NH:28][C:29](=[O:38])[C:30]1[CH:35]=[CH:34][C:33]([Br:36])=[CH:32][C:31]=1[F:37])[C:25]([OH:27])=O)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[CH2:14]([O:21][CH2:22][CH2:23][CH:24]([NH:28][C:29](=[O:38])[C:30]1[CH:35]=[CH:34][C:33]([Br:36])=[CH:32][C:31]=1[F:37])[C:25](=[O:27])[CH3:1])[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1

参加物

4

反応物 3

HCID 1049PyridineHCID 7918Acetic AnhydrideHCID 589514334-Benzyloxy-2-(4-bromo-2-fluoro-benzoylamino)-butyric acid2 回

生成物 1

HCID 58951463N-[1-(2-Benzyloxy-ethyl)-2-oxo-propyl]-4-bromo-2-fluoro-benzamide

反応条件

温度
90 °C

実験手順

Add acetic anhydride (0.97 mmol) and pyridine (0.58 mmol) to a round bottom flask containing 4-benzyloxy-2-(4-bromo-2-fluoro-benzoylamino)-butyric acid (1.0 mmol) (See Intermediate 35) and heat to 90° C. for two hours. After this time, remove the heat and concentrate in vacuo. Wash crude with 1N hydrochloric acid and water while extracting with diethyl ether. Concentrate the organics in vacuo and purify on an Isco CombiFlash® chromatography system eluting with ethyl acetate and hexane. MS (m/e) (79Br/81Br): 408.3/410.3 (M+1)

後処理

  1. customAfter this time, remove the
  2. temperatureheat
  3. concentrationconcentrate in vacuo
  4. washWash crude with 1N hydrochloric acid and water
  5. extractionwhile extracting with diethyl ether
  6. concentrationConcentrate the organics in vacuo
  7. custompurify on an Isco CombiFlash® chromatography system
  8. washeluting with ethyl acetate and hexane

出典と根拠

ORDレコード
ord-8a6c132dd22447289cb3cd365b804427
出典データセット
uspto-grants-2010_02
特許番号
US07666871B2

反応ノート

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