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Water → HCID 12112223、化合物

HRID 1168944
ノート
印刷プレビュー

反応式

HRID 1168944 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][CH:14]([CH3:16])[CH3:15])[CH:12]=1.[O:17]=[C:18]([OH:30])[C@@H:19]([C@H:21]([C@H:23]([C@@H:25]([C:27]([OH:29])=[O:28])[OH:26])[OH:24])[OH:22])[OH:20].O>C(O)C>[O:17]=[C:18]([OH:30])[C@@H:19]([C@H:21]([C@H:23]([C@@H:25]([C:27]([OH:29])=[O:28])[OH:26])[OH:24])[OH:22])[OH:20].[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][CH:14]([CH3:16])[CH3:15])[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 9794517HCID 9794517、化合物

生成物 1

HCID 12112223HCID 12112223、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of methyl(3-(5-isopropoxy-3-pyridyloxy)propyl)amine (0.643 g, 2.87 mmol) in ethanol (10.7 mL) was added galactaric acid (302.0 mg, 1.44 mmol). Water (3.0 mL) was added drop-wise, while warming the solution to near reflux. To remove some white, insoluble crystals, 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) (3.4 mL). The filtrate was diluted with ethanol (16 mL), producing a white precipitate. The mixture was allowed to cool to ambient temperature and was further cooled at 5° C. for 48 h. The precipitate was filtered, washed with ethanol (10 mL), and vacuum dried at 40° C. for 24 h to give 251.1 mg (53.2%) of a white, crystalline solid, mp 118-120° C. The compound exhibits a Ki of 21 nM; the effect at muscle sites is 22 percent; and the effect at ganglia sites is 0 percent. The compound exhibits neurotransmitter release of 36 percent.

後処理

  1. temperaturewhile warming the solution
  2. temperatureto near reflux
  3. customTo remove some white, insoluble crystals
  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, v/v) (3.4 mL)
  6. additionThe filtrate was diluted with ethanol (16 mL)
  7. customproducing a white precipitate
  8. temperaturewas further cooled at 5° C. for 48 h
  9. filtrationThe precipitate was filtered
  10. washwashed with ethanol (10 mL), and vacuum
  11. customdried at 40° C. for 24 h
  12. customto give 251.1 mg (53.2%) of a white, crystalline solid, mp 118-120° C

出典と根拠

ORDレコード
ord-2960fd3a07024608b0a2b9efa39c442c
出典データセット
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06627648B1

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