N-Aminomorpholine → 2-Hydroxy-N-(4-morpholinyl)-2-phenyl-2-(3-pyridinyl)-acetamide

HRID 22240

Reaktionsgleichung

Reaktionsgleichung von HRID 22240
[OH:1][C:2]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)([C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1)[C:3]([OH:5])=O.O.ON1C2C=CC=CC=2N=N1.[NH2:29][N:30]1[CH2:35][CH2:34][O:33][CH2:32][CH2:31]1.C(=O)(O)[O-].[Na+]>O1CCOCC1.CN(C)C=O>[OH:1][C:2]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)([C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1)[C:3]([NH:29][N:30]1[CH2:35][CH2:34][O:33][CH2:32][CH2:31]1)=[O:5]

Komponenten

7

Versuchsvorschrift

A mixture of 2-hydroxy-2-phenyl-2-(3-pyridinyl)acetic acid (3.48 g, 0. 015 mole) , 1-hyrdoxybenzotriazole hydrate (4.10 g, 0.03 mole), 1,3-Dicyclohexycarbodiimide (3.09 g, 0.015 mole), 4-aminomorpholine (1.45 ml, 0.015 mole), sodium bicarbonate (1.26 g, 0.015 mole), N,N-dimethyformamide (36 ml) and dioxane (36 ml) were stirred at room temperature overnight. The volatiles were removed in vacuo, dichloromethane (170 ml) was added and following filtration, the organic layer was washed with saturated sodium bicarbonate and brine. After drying, filtration and concentration, the residue was purified by column chromatography using 10% methanol in chloroform to give 3.92 g of the product as a white foam. High Res. Mass Spec. Calcd. for C17H19N3O3 :314.1505 (M+H). Found: 314.1501.

Aufarbeitung

  1. customThe volatiles were removed in vacuo, dichloromethane (170 ml)
  2. additionwas added
  3. filtrationfiltration
  4. washthe organic layer was washed with saturated sodium bicarbonate and brine
  5. customAfter drying
  6. filtrationfiltration and concentration
  7. customthe residue was purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-eb69e07ce28f4f7c848e864fd55145cd
Quelldatensatz
uspto-grants-1995_06
Patentnummer
US05428035

Verknüpfte Notizen

Wird geladen…