Methyl(2-(morpholin-4-yl)ethyl)amine → 6-Methoxy-N-methyl-N-[2-(4-morpholinyl)ethyl]-1,2-benzisoxazol-3-amine

HRID 582859

Reaktionsgleichung

Reaktionsgleichung von HRID 582859
Cl[C:2]1[C:6]2[CH:7]=[CH:8][C:9]([O:11][CH3:12])=[CH:10][C:5]=2[O:4][N:3]=1.[CH3:13][NH:14][CH2:15][CH2:16][N:17]1[CH2:22][CH2:21][O:20][CH2:19][CH2:18]1>>[CH3:12][O:11][C:9]1[CH:8]=[CH:7][C:6]2[C:2]([N:14]([CH3:13])[CH2:15][CH2:16][N:17]3[CH2:22][CH2:21][O:20][CH2:19][CH2:18]3)=[N:3][O:4][C:5]=2[CH:10]=1

Komponenten

3

Edukt 2

HCID 14979282Methyl(2-(morpholin-4-yl)ethyl)amineHCID 158169243-Chloro-6-methoxy-1,2-benzoxazole

Produkt 1

HCID 158169256-Methoxy-N-methyl-N-[2-(4-morpholinyl)ethyl]-1,2-benzisoxazol-3-amineAusbeute 49,4 %

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

To a sealed tube was added 3-chloro-6-methoxy-1,2-benzisoxazole (6.0 g) and N-methyl-N-[2-(4-morpholinyl)ethyl]-amine (13.8 g). The reaction was heated to 140° C. over 48 hours and then cooled to room temperature. The residue was partitioned between ethyl acetate (EtOAc) and water, extracted again with EtOAc, and the organic phase was dried over magnesium sulfate (MgSO4) and concentration in vacuo. Flash column chromatography (silica gel) eluting with 1% methanol/dichloromethane (MeOH/DCM) provided the product (4.7 g), m.p. 43-44° C.

Aufarbeitung

  1. temperaturecooled to room temperature
  2. customThe residue was partitioned between ethyl acetate (EtOAc) and water
  3. extractionextracted again with EtOAc
  4. dry with materialthe organic phase was dried over magnesium sulfate (MgSO4) and concentration in vacuo
  5. washFlash column chromatography (silica gel) eluting with 1% methanol/dichloromethane (MeOH/DCM)

Quellen und Nachweise

ORD-Eintrag
ord-011f174329cc4dd6bd4aaca930b1b5ca
Quelldatensatz
uspto-grants-1999_07
Patentnummer
US05925766

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