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

Water → Methyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amine Hemigalactarate

HRID 2305717
ノート
印刷プレビュー

反応式

HRID 2305717 の反応式
[CH3:1][NH:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[N:9][CH:10]=[C:11]([O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:12]=1.[O:21]=[C:22]([OH:34])[C@@H:23]([C@H:25]([C@H:27]([C@@H:29]([C:31]([OH:33])=[O:32])[OH:30])[OH:28])[OH:26])[OH:24].O>C(O)C>[O:21]=[C:22]([OH:34])[C@@H:23]([C@H:25]([C@H:27]([C@@H:29]([C:31]([OH:33])=[O:32])[OH:30])[OH:28])[OH:26])[OH:24].[CH3:1][NH:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[N:9][CH:10]=[C:11]([O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:12]=1.[CH3:1][NH:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[N:9][CH:10]=[C:11]([O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:12]=1
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 962WaterHCID 3037582Galactaric acidHCID 9881953Methyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amine

生成物 1

HCID 12112224Methyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amine Hemigalactarate収率 65.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of methyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)-amine (1.07 g, 3.929 mmol) in ethanol (15 mL) was added galactaric acid (0.413 g, 1.964 mmol). Water (1.5 mL) was added drop-wise, while warming the solution to reflux. To remove some white, insoluble solids, the warm solution was filtered through a glass wool plug, washing the filter plug with a warm solution of ethanol-water (4:1, v/v) (5 mL). The filtrate was diluted with ethanol (23 mL). The mixture was allowed to cool to ambient temperature; however, no solids precipitated. The solution was concentrated by rotary evaporation and briefly dried under high vacuum. The resulting brown solids were dissolved in a mixture of hot 2-propanol (˜15 mL) and water (0.8 mL); the dark-brown solution was allowed to cool to ambient temperature. After 30 min of precipitation, the batch was diluted with 2-propanol (30 mL) and stored at 5° C. for 16 h. The resulting solids were filtered, washed with cold 2-propanol (3×5 mL) and vacuum dried at 45° C. to give 0.967 g (65.2%) of a beige powder, mp 137-140° C. The compound exhibits a Ki of 2 nM; the effect at muscle sites is 1 percent; and the effect at ganglia sites is 3 percent. The compound exhibits neurotransmitter release of 38 percent.

後処理

  1. temperaturewhile warming the solution
  2. temperatureto reflux
  3. customTo remove some white, insoluble solids
  4. filtrationthe warm solution was filtered through a glass wool plug
  5. washwashing the filter plug with a warm solution of ethanol-water (4:1
  6. additionThe filtrate was diluted with ethanol (23 mL)
  7. customhowever, no solids precipitated
  8. concentrationThe solution was concentrated by rotary evaporation
  9. custombriefly dried under high vacuum
  10. dissolutionThe resulting brown solids were dissolved in a mixture of hot 2-propanol (˜15 mL) and water (0.8 mL)
  11. temperatureto cool to ambient temperature
  12. customAfter 30 min of precipitation
  13. additionthe batch was diluted with 2-propanol (30 mL)
  14. filtrationThe resulting solids were filtered
  15. washwashed with cold 2-propanol (3×5 mL) and vacuum
  16. customdried at 45° C.

出典と根拠

ORDレコード
ord-5a73a501137c412598433acc55644423
出典データセット
uspto-grants-2002_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06441006B2

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