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

Sodium Bicarbonate → HCID 22473967、化合物

HRID 2183676
ノート
印刷プレビュー

反応式

HRID 2183676 の反応式
[ClH:1].[S:2]1[CH:6]=[CH:5][C:4]2[C:7]([C:11]3[N:12]4[CH2:19][CH2:18][N:17]=[C:13]4[S:14][C:15]=3[CH3:16])=[CH:8][CH:9]=[CH:10][C:3]1=2.[C:20](=O)([O-])O.[Na+]>ClCCl>[ClH:1].[CH3:16][C:15]1[S:14][C:13]2=[N:17][CH2:18][CH2:19][N:12]2[C:11]=1[C:7]1[C:4]2[CH:5]=[C:6]([CH3:20])[S:2][C:3]=2[CH:10]=[CH:9][CH:8]=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 516892Sodium BicarbonateHCID 9857808HCID 9857808、化合物

生成物 1

HCID 22473967HCID 22473967、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A mixture of 3-(benzo[b]thiophen-4-yl)-2-methyl-5,6-dihydroimidazo[2,1-b]thiazole hydrochloride (2 g; prepared in a manner similar to that described in Example 9 Method A), 5M aqueous sodium hydrogencarbonate solution (50 ml) and dichloromethane (50 ml) was stirred at ambient temperature for 30 minutes, then the free base was extracted into dichloromethane (2×50 ml). The combined extracts were dried (MgSO4) and the solvent was removed in vacuo. The residue was dissolved in tetrahydrofuran (40 ml), then the stirred solution was cooled to −70° C. and n-butyllithium (2.5M solution in hexanes; 2.85 ml) was added dropwise under nitrogen. The mixture was stirred at −70° C. for 1 hour, then methyl iodide (0.45 ml) was added dropwise. The mixture was stirred at −70° C. for 1 hour then it was poured into saturated aqueous ammonium chloride solution (50 ml). The product was extracted into ethyl acetate (2×50 ml), the combined extracts were dried (MgSO4) and the solvents were removed in vacuo. The residue was purified via flash chromatography over silica using a 9:1 mixture of dichloromethane and methanol as eluant. Appropriate fractions were combined and the solvents were removed in vacuo. The residue was dissolved in ethanol, concentrated hydrochloric acid (10 drops) was added, the solvent was removed in vacuo, and the residue was triturated with ether (30 ml). The mixture was allowed to stand at ambient temperature for 72 hours then the resulting solid was collected by filtration and dried in vacuo to give 2-methyl-3-(2-methylbenzo[b]thiophen-4-yl)-5,6-dihydroimidazo[2,1-b]thiazole hydrochloride (1.15 g) as a colourless solid, m.p. 271° C.

後処理

  1. customprepared in a manner similar to
  2. extractionthe free base was extracted into dichloromethane (2×50 ml)
  3. dry with materialThe combined extracts were dried (MgSO4)
  4. customthe solvent was removed in vacuo
  5. dissolutionThe residue was dissolved in tetrahydrofuran (40 ml)
  6. temperaturethe stirred solution was cooled to −70° C.
  7. additionn-butyllithium (2.5M solution in hexanes; 2.85 ml) was added dropwise under nitrogen
  8. stirringThe mixture was stirred at −70° C. for 1 hour
  9. additionmethyl iodide (0.45 ml) was added dropwise
  10. stirringThe mixture was stirred at −70° C. for 1 hour
  11. additionit was poured into saturated aqueous ammonium chloride solution (50 ml)
  12. extractionThe product was extracted into ethyl acetate (2×50 ml)
  13. dry with materialthe combined extracts were dried (MgSO4)
  14. customthe solvents were removed in vacuo
  15. customThe residue was purified via flash chromatography over silica using
  16. additiona 9:1 mixture of dichloromethane and methanol as eluant
  17. customthe solvents were removed in vacuo
  18. dissolutionThe residue was dissolved in ethanol
  19. additionconcentrated hydrochloric acid (10 drops) was added
  20. customthe solvent was removed in vacuo
  21. customthe residue was triturated with ether (30 ml)
  22. waitto stand at ambient temperature for 72 hours
  23. filtrationthe resulting solid was collected by filtration
  24. customdried in vacuo

出典と根拠

ORDレコード
ord-6805a904446d44a9a7863e69a0f5f354
出典データセット
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06900216B2

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