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Ammonium Chloride → 4-{4-[(4-methylpiperazin-1-yl)methyl]tetrahydro-2H-pyran-4-yl}phenol

HRID 273003
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 273003
C[S-].[Na+].C[O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2([CH2:18][N:19]3[CH2:24][CH2:23][N:22]([CH3:25])[CH2:21][CH2:20]3)[CH2:17][CH2:16][O:15][CH2:14][CH2:13]2)=[CH:8][CH:7]=1.[Cl-].[NH4+]>CN(C)C=O>[CH3:25][N:22]1[CH2:21][CH2:20][N:19]([CH2:18][C:12]2([C:9]3[CH:8]=[CH:7][C:6]([OH:5])=[CH:11][CH:10]=3)[CH2:13][CH2:14][O:15][CH2:16][CH2:17]2)[CH2:24][CH2:23]1
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Komponenten

5

Edukt 3

HCID 25517Ammonium ChlorideHCID 4378561Sodium methanethiolateHCID 685756701-{[4-(4-methoxyphenyl)tetrahydro-2H-pyran-4-yl]methyl}4-methylpiperazine

Produkt 1

HCID 685768084-{4-[(4-methylpiperazin-1-yl)methyl]tetrahydro-2H-pyran-4-yl}phenolAusbeute 103,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
130 °C

Versuchsvorschrift

To a suspension of sodium thiomethoxide (660 mg, 9.4 mmol) in N,N-dimethylformamide (2 ml) was added 1-{[4-(4-methoxyphenyl)tetrahydro-2H-pyran-4-yl]methyl}4-methylpiperazine (410 mg, 1.3 mmol) in N,N-dimethylformamide (3 ml). The reaction mixture was heated to 130° C. under nitrogen for 18 hours. The mixture was then allowed to cool down to room temperature and saturated aqueous ammonium chloride was added. The mixture was extracted with ethyl acetate (2×30 ml). The combined organic extracts were dried over sodium sulphate, filtered and concentrated in vacuo to provide a pale brown oil. This was azeotroped with toluene and dried under high vacuum to provide the title compound (390 mg, 100%) as an off-white solid. HRMS ESI+ m/z 291.2062 [MH]+.

Aufarbeitung

  1. temperatureto cool down to room temperature
  2. extractionThe mixture was extracted with ethyl acetate (2×30 ml)
  3. dry with materialThe combined organic extracts were dried over sodium sulphate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customto provide a pale brown oil
  7. customThis was azeotroped with toluene
  8. customdried under high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-5a2bdd95eef6439992dd03c805fd6110
Quelldatensatz
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07456164B2

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