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

Ethyl 5-methoxyimidazo[1,2-a]quinoline-2-carboxylate → HCID 13055757、化合物

HRID 2166510
ノート
印刷プレビュー

反応式

HRID 2166510 の反応式
[CH3:1][O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[N:6]2[CH:13]=[C:14]([C:16](OCC)=[O:17])[N:15]=[C:5]2[CH:4]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[CH3:1][O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[N:6]2[CH:13]=[C:14]([CH2:16][OH:17])[N:15]=[C:5]2[CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 13055756Ethyl 5-methoxyimidazo[1,2-a]quinoline-2-carboxylateHCID 21226445Aluminium lithium hydride

生成物 1

HCID 13055757HCID 13055757、化合物収率 89.2%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A suspension of 19.71 g (73 mmol) of ethyl 5-methoxyimidazo[1,2-a]quinoline-2-carboxylate in 350 ml of freshly distilled anhydrous tetrahydrofuran was stirred under a nitrogen atmosphere at room temperature and 3.33 g (88 mmol) of lithium aluminum hydride were added thereto in portions over 3 hours. The mixture was stirred for 4 hours and excess hydride was destroyed by dropwise addition of wet tetrahydrofuran followed by water. The mixture was poured into 1.5 liters of water and the mixture was extracted with 500 ml of a chloroform-methanol mixture. The mixture was filtered through a celite pad and the aqueous phase was extracted again with a chloroform-methanol mixture. The combined organic phases were dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure. The residue was triturated with ethyl acetate, filtered, washed with ethyl acetate and dried under reduced pressure over P2O5 to obtain 14.87 g (89% yield) of 5-methoxy-imidazo[1,2-a]quinoline-2-methanol as a white crystalline solid melting at 173°-175° C.

後処理

  1. stirringThe mixture was stirred for 4 hours
  2. customexcess hydride was destroyed by dropwise addition of wet tetrahydrofuran
  3. additionThe mixture was poured into 1.5 liters of water
  4. extractionthe mixture was extracted with 500 ml of a chloroform-methanol mixture
  5. filtrationThe mixture was filtered through a celite pad
  6. extractionthe aqueous phase was extracted again with a chloroform-methanol mixture
  7. dry with materialThe combined organic phases were dried over anhydrous magnesium sulfate
  8. customevaporated to dryness under reduced pressure
  9. customThe residue was triturated with ethyl acetate
  10. filtrationfiltered
  11. washwashed with ethyl acetate
  12. dry with materialdried under reduced pressure over P2O5

出典と根拠

ORDレコード
ord-faf7a24c59de4f2788d8691028865a32
出典データセット
uspto-grants-1983_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04387098

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