Water → Dimethyl(4-(3-pvridyloxy)butyl)amine Hemigalactarate

HRID 2305704노트

반응식

HRID 2305704 반응식
[CH3:1][N:2]([CH3:14])[CH2:3][CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=1.[O:15]=[C:16]([OH:28])[C@@H:17]([C@H:19]([C@H:21]([C@@H:23]([C:25]([OH:27])=[O:26])[OH:24])[OH:22])[OH:20])[OH:18].O>C(O)C>[O:15]=[C:16]([OH:28])[C@@H:17]([C@H:19]([C@H:21]([C@@H:23]([C:25]([OH:27])=[O:26])[OH:24])[OH:22])[OH:20])[OH:18].[CH3:14][N:2]([CH3:1])[CH2:3][CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=1.[CH3:1][N:2]([CH2:3][CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=1)[CH3:14]

참가 물질

5

반응물 3

HCID 962WaterHCID 3037582Galactaric acidHCID 9794168Dimethyl(4-(3-pyridyloxy)butyl)amine

생성물 1

HCID 131723460Dimethyl(4-(3-pvridyloxy)butyl)amine Hemigalactarate

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of dimethyl(4-(3-pyridyloxy))butylamine (1.26 g, 6.49 mmol) in ethanol (10 mL) was added galactaric acid (0.682 g, 3.25 mmol). Water (3 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) (4 mL). The filtrate was diluted with ethanol (80 mL). The mixture was allowed to cool to ambient temperature and was further cooled at 5° C. for 16 h. Very few solids precipitated. Consequently, the solution was concentrated, and the residue was slurried in ether. The solids were filtered, washed with ether and vacuum dried at 40° C. to give 1.06 g (54.7%) of a light-brown, flaky powder, mp 127-130° C. The compound exhibits a Ki of 3410 nM. The compound exhibits neurotransmitter release of 24 percent.

후처리

  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 (80 mL)
  7. temperaturewas further cooled at 5° C. for 16 h
  8. customVery few solids precipitated
  9. concentrationConsequently, the solution was concentrated
  10. filtrationThe solids were filtered
  11. washwashed with ether and vacuum
  12. customdried at 40° C.
  13. customto give 1.06 g (54.7%) of a light-brown, flaky powder, mp 127-130° C

출처 및 근거

ORD 기록
ord-71dfa72abba641bcbeff9febe1715d0c
출처 데이터셋
uspto-grants-2002_08
특허 번호
US06441006B2

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