ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

1-Bromo-3-chloropropane → 5-Chloro-1-(3-chloropropyl)-3,4-dihydrocarbostyril

HRID 2256982
ノート
印刷プレビュー

反応式

HRID 2256982 の反応式
[H-].[Na+].[Cl:3][C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH2:6][CH2:7][C:8](=[O:14])[NH:9]2.Br[CH2:16][CH2:17][CH2:18][Cl:19]>CN(C=O)C>[Cl:3][C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH2:6][CH2:7][C:8](=[O:14])[N:9]2[CH2:16][CH2:17][CH2:18][Cl:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 80061-Bromo-3-chloropropaneHCID 24758Sodium hydrideHCID 190277365-chloro-3,4-dihydroquinolin-2(1H)-one

生成物 1

HCID 153840875-Chloro-1-(3-chloropropyl)-3,4-dihydrocarbostyril

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

In the same manner as in Reference Example 1, 60% sodium hydride in oil was added portionwise to a solution of 5-chloro-3,4-dihydrocarbostyril in DMF, the resultant mixture was stirred for 30 minutes, 1-bromo-3-chloropropane was then added, and the resultant mixture was further stirred at 80°-90° C. for 8 hours. The DMF was distilled off under reduced pressure, and the residue was extracted with chloroform. The extract was washed with water and dried (anhydrous magnesium sulfate), the chloroform was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography to give 5-chloro-1-(3-chloropropyl)-3,4-dihydrocarbostyril as a pale yellow oil.

後処理

  1. distillationThe DMF was distilled off under reduced pressure
  2. extractionthe residue was extracted with chloroform
  3. washThe extract was washed with water
  4. dry with materialdried (anhydrous magnesium sulfate)
  5. distillationthe chloroform was distilled off under reduced pressure
  6. customthe residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-535407ebb61b41e0923bfe11451cdb65
出典データセット
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05656633

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート