Pyridine → 7-(2-Bromobenzoylamino)quinoline-3-carboxylic acid ethyl ester

HRID 51919

反応式

HRID 51919 の反応式
[Br:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4](Cl)=[O:5].[NH2:11][C:12]1[CH:21]=[C:20]2[C:15]([CH:16]=[C:17]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH:18]=[N:19]2)=[CH:14][CH:13]=1.N1C=CC=CC=1>C(Cl)(Cl)Cl>[CH2:25]([O:24][C:22]([C:17]1[CH:18]=[N:19][C:20]2[C:15]([CH:16]=1)=[CH:14][CH:13]=[C:12]([NH:11][C:4](=[O:5])[C:3]1[CH:7]=[CH:8][CH:9]=[CH:10][C:2]=1[Br:1])[CH:21]=2)=[O:23])[CH3:26]

参加物

5

反応物 3

HCID 1049PyridineHCID 235422-Bromobenzoyl chlorideHCID 9877801Ethyl 7-aminoquinoline-3-carboxylate

生成物 1

HCID 698911587-(2-Bromobenzoylamino)quinoline-3-carboxylic acid ethyl ester収率 50%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒2 回

実験手順

A solution of 2-Bromobenzoyl chloride (5.38 g, 24.5 mmol) in 100 ml chloroform was added dropwise at room temperature to a solution of ethyl 7-aminoquinoline-3-carboxylate (2.65 g, 12.25 mmol), 4-N,N-dimethylaminopyridine (150 mg, 1.23 mmol) and pyridine (3.96 ml, 49 mmol) in 100 ml chloroform. The resulting solution was heated under reflux for 4 hr, then cooled to room temperature. The chloroform solution was then washed sequentially with dilute aqueous hydrochloric acid solution, water and brine, dried over anhydrous sodium sulfate and concentrated to dryness in vacuo. The residue was chromatographed on silica gel, eluting with 60:40 hexane/ethyl acetate to yield the title product as a solid foam (2.45 g 50% yield).

後処理

  1. temperatureThe resulting solution was heated
  2. temperatureunder reflux for 4 hr
  3. washThe chloroform solution was then washed sequentially with dilute aqueous hydrochloric acid solution, water and brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated to dryness in vacuo
  6. customThe residue was chromatographed on silica gel
  7. washeluting with 60:40 hexane/ethyl acetate

出典と根拠

ORDレコード
ord-515124e287874ebd87ffdaa652a8f319
出典データセット
uspto-grants-2004_03
特許番号
US06713489B2

関連ノート

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