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Isocyanate → (2S,5R)-1-benzyl-2,5-dimethyl-4-(tetrahydro-2H-pyran-4-yl)piperazine

HRID 331077
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 331077
[CH2:1]([N:8]1[CH2:13][C@@H:12]([CH3:14])[NH:11][CH2:10][C@@H:9]1[CH3:15])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[O:16]1[CH2:21][CH2:20][C:19](=O)[CH2:18][CH2:17]1.[BH3-]C#N.[Na+].[N-]=C=O>C1COCC1.CCO>[CH2:1]([N:8]1[CH2:13][C@@H:12]([CH3:14])[N:11]([CH:19]2[CH2:20][CH2:21][O:16][CH2:17][CH2:18]2)[CH2:10][C@@H:9]1[CH3:15])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 105034IsocyanateHCID 121599Tetrahydro-4H-pyran-4-oneHCID 5003444Sodium cyanoborohydrideHCID 23402345(2S,5R)-1-Benzyl-2,5-dimethylpiperazine

Produkt 1

HCID 59334017(2S,5R)-1-benzyl-2,5-dimethyl-4-(tetrahydro-2H-pyran-4-yl)piperazineAusbeute 84 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702
Ethanol
Lösungsmittel
HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a mixture of (2S,5R)-1-benzyl-2,5-dimethylpiperazine (11.0 g, 53.8 mmol) and of tetrahydro-4H-pyran-4-one (5.39 g, 53.8 mmol) at 0° C. was added Ti(IV) isopropoxide (19.2 mL, 67.3 mmol). The resulting mixture was stirred at rt overnight and an orange suspension was obtained. To the suspension was added EtOH (25 mL) and NaCNBH3 (4.27 g, 64.6 mmol, 1.20 eq). The resulting mixture was stirred at rt for 24 h. The reaction mixture was then quenched with water (5.0 mL) and a yellow solid was generated. The suspension was diluted with EtOAc (400 mL) and filtered. The filtrate was concentrated under reduced pressure. The residue was again diluted with EtOAc (500 mL), dried over Na2SO4, and filtered. The filtrate was collected and concentrated under reduced pressure to afford a yellow oil. The oil was diluted in THF (400 mL) and PS-isocyanate was added to remove secondary amine. The suspension was filtered and the filtrate concentrated. The residue was purified by column chromatography using 50:5:1 CHCl3/MeOH/Et3N to afford the desired compound as yellow oil (13.0 g, 84%)

Aufarbeitung

  1. customan orange suspension was obtained
  2. stirringThe resulting mixture was stirred at rt for 24 h
  3. customThe reaction mixture was then quenched with water (5.0 mL)
  4. additionThe suspension was diluted with EtOAc (400 mL)
  5. filtrationfiltered
  6. concentrationThe filtrate was concentrated under reduced pressure
  7. additionThe residue was again diluted with EtOAc (500 mL)
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. customThe filtrate was collected
  11. concentrationconcentrated under reduced pressure
  12. customto afford a yellow oil
  13. customto remove secondary amine
  14. filtrationThe suspension was filtered
  15. concentrationthe filtrate concentrated
  16. customThe residue was purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-891eeedd9aca48aa80cc2734d6062d6b
Quelldatensatz
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08877761B2

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